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Check Valve (Fitting)

by Merit Medical Systems, Inc.

510(k) K933084

Check Valve (Fitting) is a Class II device made by Merit Medical Systems, Inc., cleared under FDA 510(k) K933084 on 23 Mar 1994, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK933084 Date23 Mar 1994ClearedStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
DTL
Device class
Class II
Regulation
21 CFR Part 870.4290
Advisory committee
Cardiovascular
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code DTL (Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass).

Other devices from Merit Medical Systems, Inc.

See all devices from Merit Medical Systems, Inc. →