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Cardinal Health WHSA30MMB

by Cardinal Health 200, LLC

Cardinal Health WHSA30MMB is a Class II device made by Cardinal Health 200, LLC, cleared under FDA 510(k) K930957 on 2 Jul 1993 and listed in FDA GUDID since 30 Oct 2025 (UDI-DI 50885380208506), 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

510(k) K930957

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number50885380208506 UDI-DI Date30 Oct 2025ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESK from GUDID Substantially Equivalent — Kit · Traditional NumberK930957 Date2 Jul 1993DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K930957 decided 2 Jul 1993 Active
  • FDA GUDID UDI-DI 50885380208506 listed 30 Oct 2025 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K930957
  2. Listed FDA GUDID 50885380208506

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Cardinal Health
Generic name
Microbial medical gas filter, single-use
Model / Ref / Catalog
WHSA30MMB
Primary DI / UDI-DI
50885380208506
510(k) Number
FDA product code
CCK
GMDN term
Microbial medical gas filter, single-use
Device class
Class II
Regulation number
868.1400
GUDID distribution status
In Commercial Distribution
Size
Length — 10 Feet

Related devices

Cleared under the same submission (K930957)

and 8 more cleared under K930957

Other devices from Cardinal Health 200, LLC

See all devices from Cardinal Health 200, LLC →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)