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Clip Gun CM8902

by Medtronic PS Medical

Clip Gun CM8902 is a Class II device made by Medtronic PS Medical, cleared under FDA 510(k) K896723 on 23 Mar 1990 and listed in FDA GUDID since 13 Jun 2016 (UDI-DI 20643169109135), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K896723

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number20643169109135 UDI-DI Date13 Jun 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK896723 Date23 Mar 1990DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K896723 decided 23 Mar 1990 Active
  • FDA GUDID UDI-DI 20643169109135 listed 13 Jun 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K896723
  2. Listed FDA GUDID 20643169109135

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Clip Gun
Generic name
Scalp clip applier, single-use
Model / reference
CM8902
Primary DI / UDI-DI
20643169109135
510(k) Number
FDA product code
HBO
GMDN term
Scalp clip applier, single-use
Device class
Class II
Regulation number
882.4150
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HBO (CLIP, SCALP).

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
Other properties (11, all answered No)