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Lifeguard H787LG19750

by Angiodynamics, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None ongoing

3 closed

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 Number05051684018572 UDI-DI Date23 Jun 2026ListedStatusListed GUDID: in commercial distribution

Recalls

3 recalls · FDA

    • Terminated Z-0679-2018 FDA Class II initiated 24 Jul 2017

    Vygon is conducting a voluntary recall of the products and lots listed in this recall, being initiated because our Tyvek supplier has notified Vygon of issues with their product, specifically the Tyvek may not be coated completely causing gaps in the adhesive used to seal the product packaging. This potential lack of adhesive may affect the sterility of the product.

    • Terminated Z-0914-2013 FDA Class II initiated 21 Jan 2013

    The label on the device states that the item number is CLGY-2210 when the item number on the device label should read CLGY-2010. This is a 20Ga Huber needle set; however, the product label states the pouch contains a 22Ga set.

    • Terminated Z-1327-2011 FDA Unclassified (pre-2012) initiated 16 Nov 2010

    Routine testing conducted to challenge the success of sterilization was not fully completed for sterile products.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Lifeguard
Generic Name
Vascular port administration set
Model / Ref / Catalog
H787LG19750, LG-19-75
Primary DI / UDI-DI
05051684018572
510(k) Number
FDA Product Code
FPA
GMDN Term
Vascular port administration set
Device Class
Class II
Regulation Number
880.5440
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional
Size
Length — 0.75 Inch

Related devices

Cleared under the same submission (K013871)

Show all (12)

Other devices from Angiodynamics, Inc.

See all devices from Angiodynamics, Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No