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Carter-Thomason Needle-Point Suture Passer Instrument Set

by Louisville Laboratories, Inc.

510(k) K980123

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

1 ongoing

This device is named in the recall

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 NumberK980123 Date9 Mar 1998ClearedStatusActive

Recalls

1 recall · 1 ongoing · FDA

    • Ongoing Z-0985-2024 FDA Class II initiated 29 Aug 2023

    Incorrect component descriptions within the "Contents" section on the Tyvek lid for individual kit trays.

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  • Withdrawn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
GCJ
Device Class
Class II
Regulation
21 CFR Part 876.1500
Advisory Committee
Gastroenterology, Urology
FDA Decision
SESE Substantially Equivalent

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