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Video System Center Cv-170

by Olympus Medical Systems Corporation

Video System Center Cv-170 is a Class II device made by Olympus Medical Systems Corporation, cleared under FDA 510(k) K122831 on 14 Dec 2012 and listed in FDA GUDID since 17 Dec 2021 (UDI-DI 04953170338496), active as of 22 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 22 Oct 2026

Documents

510(k) K122831

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04953170338496 UDI-DI Date17 Dec 2021ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK122831 Date14 Dec 2012DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K122831 decided 14 Dec 2012 Active
  • FDA GUDID UDI-DI 04953170338496 listed 17 Dec 2021 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K122831
  2. Listed FDA GUDID 04953170338496

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Video System Center
Generic name
Endoscopic video image processing/light source system
Model / reference
CV-170
Primary DI / UDI-DI
04953170338496
FDA product code
NTN, NWB, FET
GMDN term
Endoscopic video image processing/light source system
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

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Properties

  • Serial number
  • Manufacturing date
Other properties (13, all answered No)