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LifeVac EMS KIT LVC3002

by Lifevac, LLC

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB712LVC3002 UDI-DI Date25 Sep 2020ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
LifeVac EMS KIT
Generic Name
Emergency airway clearance suction plunger
Model / Reference
LVC3002
Primary DI / UDI-DI
B712LVC3002
FDA Product Code
GCX
GMDN Term
Emergency airway clearance suction plunger
Device Class
Class II
Regulation Number
880.6740
GUDID distribution status
Not in Commercial Distribution

Related devices

Category: Emergency airway clearance suction plunger

Other devices from Lifevac, LLC

Properties

  • Single Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No