<?xml version='1.0' encoding='UTF-8'?><device xmlns='http://www.fda.gov/cdrh/gudid' xmlns:xsi='http://www.w3.org/2001/XMLSchema-instance'><publicDeviceRecordKey>a5a5a2a3-d9b9-41b4-be58-925ff8d9e9d0</publicDeviceRecordKey><publicVersionStatus>Update</publicVersionStatus><deviceRecordStatus>Published</deviceRecordStatus><publicVersionNumber>3</publicVersionNumber><publicVersionDate>2026-05-06</publicVersionDate><devicePublishDate>2020-09-25</devicePublishDate><deviceCommDistributionEndDate>2026-03-04</deviceCommDistributionEndDate><deviceCommDistributionStatus>Not in Commercial Distribution</deviceCommDistributionStatus><identifiers><identifier><deviceId>B712LVC3003</deviceId><deviceIdType>Primary</deviceIdType><deviceIdIssuingAgency>HIBCC</deviceIdIssuingAgency><containsDINumber xsi:nil="true"/><pkgQuantity xsi:nil="true"/><pkgDiscontinueDate xsi:nil="true"/><pkgStatus xsi:nil="true"/><pkgType xsi:nil="true"/></identifier></identifiers><brandName>LifeVac School KIT</brandName><versionModelNumber>LVC3003</versionModelNumber><catalogNumber xsi:nil="true"/><dunsNumber>071298464</dunsNumber><companyName>LIFEVAC, INC.</companyName><deviceCount>1</deviceCount><deviceDescription xsi:nil="true"/><DMExempt>false</DMExempt><premarketExempt>false</premarketExempt><deviceHCTP>false</deviceHCTP><deviceKit>true</deviceKit><deviceCombinationProduct>false</deviceCombinationProduct><singleUse>true</singleUse><lotBatch>true</lotBatch><serialNumber>false</serialNumber><manufacturingDate>false</manufacturingDate><expirationDate>false</expirationDate><donationIdNumber>false</donationIdNumber><labeledContainsNRL>false</labeledContainsNRL><labeledNoNRL>true</labeledNoNRL><MRISafetyStatus>Labeling does not contain MRI Safety Information</MRISafetyStatus><rx>false</rx><otc>false</otc><contacts><customerContact><phone>+1-516-965-1900</phone><phoneExtension xsi:nil="true"/><email>soliveri@lifevac.net</email></customerContact></contacts><gmdnTerms><gmdn><gmdnCode>63287</gmdnCode><gmdnPTName>Emergency airway clearance suction plunger</gmdnPTName><gmdnPTDefinition>A noninvasive, manual device designed for the emergency removal of an airway-obstructing object or material in the oropharynx, trachea, or bronchi to prevent patient asphyxiation. It is in the form of a compression tank (plunger) connected to a face-fitting mask that is applied to the mouth area; the plunger is manually compressed and expanded to provide a negative pressure within the airway to suck out the obstructing material. This is a single-use device.</gmdnPTDefinition><implantable>false</implantable><gmdnCodeStatus>Active</gmdnCodeStatus></gmdn></gmdnTerms><productCodes><fdaProductCode><productCode>GCX</productCode><productCodeName>Apparatus, Suction, Operating-Room, Wall Vacuum Powered</productCodeName></fdaProductCode></productCodes><deviceSizes/><environmentalConditions/><sterilization><deviceSterile>false</deviceSterile><sterilizationPriorToUse>false</sterilizationPriorToUse><methodTypes/></sterilization></device>