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Truwave, Vamp PXVK0387

by Edwards Lifesciences LLC

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

2 ongoing

Recall on shared 510(k) K142749; other models may be affected

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 StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK173586 Date5 Apr 2018DecidedStatusActive
United StatesGUDID listing Number07460691954540 UDI-DI Date3 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Recalls

12 recalls · 2 ongoing · FDA

  • 2 recalls, same reason

    • Ongoing Z-0414-2024 FDA Class II initiated 4 Oct 2023 on shared 510(k) K142749
    • Ongoing Z-0413-2024 FDA Class II initiated 4 Oct 2023 on shared 510(k) K142749

    Their is the potential for flushing difficulties during setup of the pressure monitoring kit with pressure transducer.

  • 8 recalls, same reason

    • Terminated Z-1959-2021 FDA Class II initiated 26 May 2021
    • Terminated Z-1965-2021 FDA Class II initiated 26 May 2021
    • Terminated Z-1964-2021 FDA Class II initiated 26 May 2021
    • Terminated Z-1960-2021 FDA Class II initiated 26 May 2021
    • Terminated Z-1961-2021 FDA Class II initiated 26 May 2021
    • Terminated Z-1966-2021 FDA Class II initiated 26 May 2021
    • Terminated Z-1962-2021 FDA Class II initiated 26 May 2021
    • Terminated Z-1963-2021 FDA Class II initiated 26 May 2021

    There is a potential that the pressure tubing may detach from the blood sampling system

    • Terminated Z-2776-2015 FDA Class II initiated 31 Jul 2015

    Flow restriction issues in a trifurcated IV set included in the pressure transducer kits. A restriction of the flow of IV fluid would result in either an inability to prime the system before use or difficulty in flushing the line after a blood draw.

    • Terminated Z-1146-2013 FDA Class II initiated 30 Jan 2013

    The device is being recalled because the firm has received multiple complaints related to incorrect assembly that may result in dilution of blood samples.

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Truwave, Vamp
Generic name
Arterial blood sampling kit
Model / Ref / Catalog
PXVK0387
Primary DI / UDI-DI
07460691954540
510(k) Number
FDA product code
KRA, DXO
GMDN term
Arterial blood sampling kit
Device class
Class II
Regulation number
870.1210, 870.2870
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional
Size
Total Volume — 3 Milliliter

Related devices

Category: Invasive-pressure external transducer, single-useArterial blood sampling kit

Cleared under the same submission (K142749)

Show all (12)

Cleared under the same submission (K173586)

Show all (12)

Cleared under the same submission (K896819)

Show all (12)

Other devices from Edwards Lifesciences LLC

See all devices from Edwards Lifesciences LLC →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit

Other properties (11)

  • Sterilise before use: No
  • Implantable: No
  • Contains latex: No
  • Over-the-counter: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No
  • Lot / batch number: No
  • Serial number: No
  • Expiration date: No
  • Manufacturing date: No