Skip to content

Video System Center

by Olympus Medical Systems Corp.

510(k) K122831

Video System Center is a Class II device made by Olympus Medical Systems Corp., cleared under FDA 510(k) K122831 on 14 Dec 2012, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK122831 Date14 Dec 2012ClearedStatusActive

Official records

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  • Withdrawn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
NTN
Device class
Class II
Regulation
21 CFR Part 876.1500
Advisory committee
Gastroenterology, Urology
FDA decision
SESE Substantially Equivalent

Related clearances

cited in the FDA summary

Clearances this device's FDA summary refers to, and clearances whose summaries refer to it: a citation, not a claim of equivalence.

Cites

Cited by

Source: 510k-lineage (choiben314), CC BY 4.0

Devices cleared under K122831

2 devices · FDA GUDID

Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.

Devices cleared under K122831
UDI-DISize and differences
VIDEO SYSTEM CENTER CV-170
Olympus Medical Systems Corporation
CV-17004953170338496
Prescription: no
On the market
VIDEO SYSTEM CENTER Type A OLYMPUS CV-170
Olympus Medical Systems Corporation
OLYMPUS CV-17004953170338502
Prescription: yes
On the market

Similar devices

Other devices filed under FDA product code NTN (Led Light Source).

Other devices from Olympus Medical Systems Corporation

See all devices from Olympus Medical Systems Corporation →