McKesson 796

by Mckesson Medical-Surgical Inc.

McKesson 796 is a diagnostic spirometer (FDA Class II; FDA product code BZG, Spirometer, Diagnostic) made by Mckesson Medical-Surgical Inc., cleared under FDA 510(k) K090034 on 2 Jun 2009 and listed in FDA GUDID since 9 Dec 2016 (UDI-DI 20612479194438), 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	Number20612479194438 UDI-DI	Date9 Dec 2016Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK090034	Date2 Jun 2009Decided	StatusActive

Official records

AccessGUDID record UDI-DI 20612479194438
FDA 510(k) database 510(k) number K090034

Across registries

2 registries list this device

FDA 510(k) K090034 decided 2 Jun 2009 Active
FDA GUDID UDI-DI 20612479194438 listed 9 Dec 2016 Listed

Timeline

2 dated events

2 Jun 2009 Cleared FDA 510(k) K090034
9 Dec 2016 Listed FDA GUDID 20612479194438

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: McKesson
Generic name: Diagnostic spirometer, professional
Model / reference: 796

Primary DI / UDI-DI: 20612479194438
510(k) Number: K090034
FDA product code: BZG
GMDN term: Diagnostic spirometer, professional

Device class: Class II
Regulation number: 868.1840
GUDID distribution status: In Commercial Distribution

Other devices from Mckesson Medical-Surgical Inc.

See all devices from Mckesson Medical-Surgical Inc. →

Properties

Prescription use
Lot / batch number
Serial number

Other properties (12, all answered No)