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Vamp 48VMP160

by Becton, Dickinson and Company

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

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 26 Oct 2026

Documents

510(k) K173586

FDA submission, from GUDID

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 26 Oct 2026. What this means

Regulatory status

as of registry sync 26 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00885403523611 UDI-DI Date8 Sep 2026ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK173586 Date5 Apr 2018DecidedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 26 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Vamp
Generic name
Arterial blood sampling kit
Model / Ref / Catalog
48VMP160
Primary DI / UDI-DI
00885403523611
510(k) Number
FDA product code
DXO, KRA
GMDN term
Arterial blood sampling kit
Device class
Class II
Regulation number
870.2870, 870.1210
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe
Size
Length — 150 Centimeter

Related devices

Cleared under the same submission (K173586)

Show all (12)

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
  • Manufacturing date

Other properties (8)

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