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4F-7F Medi-Dyne Torq Flow Xlb Angiographic Catheter

by Medi-Dyne, Inc.

510(k) K000825

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

1 closed

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK000825 Date21 Sep 2000ClearedStatusActive

Recalls

1 recall · FDA

    • Terminated Z-0593-03 FDA Unclassified (pre-2012) initiated 21 Nov 2002 on shared 510(k) K000825

    6 Fr. catheters packaged and labeled as 5 Fr.

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

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  • Withdrawn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
DQO
Device Class
Class II
Regulation
21 CFR Part 870.1200
Advisory Committee
Cardiovascular
FDA Decision
SESE Substantially Equivalent

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