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Vasoview 5 Harvesting Cannula

by Guidant Corporation, Cardiac Surgery

510(k) K020143

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 NumberK020143 Date20 Feb 2002ClearedStatusActive

Recalls

1 recall · FDA

    • Terminated Z-0292-04 FDA Unclassified (pre-2012) initiated 19 Nov 2003

    VasoView 5 scissors are stiff and/or the scissor toggle has the potential to break during use.

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  • Withdrawn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
HET
Device Class
Class II
Regulation
21 CFR Part 884.1720
Advisory Committee
Obstetrics/Gynecology
FDA Decision
SESE Substantially Equivalent

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