McKesson 16-NBCH22GS

by Mckesson Medical-Surgical Inc.

McKesson 16-NBCH22GS is a Class II device made by Mckesson Medical-Surgical Inc., cleared under FDA 510(k) K172763 on 4 Jun 2018 and listed in FDA GUDID since 26 Jun 2019 (UDI-DI 20612479244423), active as of 23 Oct 2026.

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 23 Oct 2026

Documents

FDA submission, from GUDID

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number20612479244423 UDI-DI	Date26 Jun 2019Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k) from GUDID	NumberK172763	Date4 Jun 2018Issued	StatusActive

Official records

AccessGUDID record UDI-DI 20612479244423
FDA 510(k) database 510(k) number K172763

Across registries

2 registries list this device

FDA 510(k) K172763 decided 4 Jun 2018 Active
FDA GUDID UDI-DI 20612479244423 listed 26 Jun 2019 Listed

Timeline

2 dated events

4 Jun 2018 Cleared FDA 510(k) K172763
26 Jun 2019 Listed FDA GUDID 20612479244423

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: McKesson
Generic name: Non-fixed blood collection needle
Model / reference: 16-NBCH22GS

Primary DI / UDI-DI: 20612479244423
510(k) Number: K172763
FDA product code: FMI
GMDN term: Non-fixed blood collection needle

Device class: Class II
Regulation number: 880.5570
GUDID distribution status: In Commercial Distribution

Similar devices in this category

Other devices filed under Non-fixed blood collection needle.

Other devices from Mckesson Medical-Surgical Inc.

See all devices from Mckesson Medical-Surgical Inc. →

Properties

Supplied sterile
Single use
Prescription use
Lot / batch number
Expiration date

Other properties (10, all answered No)