Skip to content

Diatek Cannon-Catheter, Model CC5500

by Arrow Intl., Inc.

510(k) K022662

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

8 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)SESK Substantially Equivalent — Kit · Traditional NumberK022662 Date9 May 2003ClearedStatusActive

Recalls

8 recalls · FDA

  • 8 recalls, same reason

    • Terminated Z-2245-2008 FDA Unclassified (pre-2012) initiated 10 Jun 2008
    • Terminated Z-2247-2008 FDA Unclassified (pre-2012) initiated 10 Jun 2008
    • Terminated Z-2248-2008 FDA Unclassified (pre-2012) initiated 10 Jun 2008
    • Terminated Z-2250-2008 FDA Unclassified (pre-2012) initiated 10 Jun 2008
    • Terminated Z-2251-2008 FDA Unclassified (pre-2012) initiated 10 Jun 2008
    • Terminated Z-2246-2008 FDA Unclassified (pre-2012) initiated 10 Jun 2008
    • Terminated Z-2244-2008 FDA Unclassified (pre-2012) initiated 10 Jun 2008
    • Terminated Z-2243-2008 FDA Unclassified (pre-2012) initiated 10 Jun 2008

    The tips may not have been adequately welded to the catheter body.

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  • Withdrawn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
MSD
Device Class
Class II
Regulation
21 CFR Part 876.5540
Advisory Committee
Gastroenterology, Urology
FDA Decision
SESK Substantially Equivalent — Kit

Other devices from Arrow Intl., Inc.

See all devices from Arrow Intl., Inc. →