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Cordis Obturator

by Cordis Corp.

510(k) K914352

Cordis Obturator is a Class II device made by Cordis Corp., cleared under FDA 510(k) K914352 on 22 Nov 1991, 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 NumberK914352 Date22 Nov 1991ClearedStatusActive

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  • Withdrawn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
DYB
Device class
Class II
Regulation
21 CFR Part 870.1340
Advisory committee
Cardiovascular
FDA decision
SESE Substantially Equivalent

Devices cleared under K914352

5 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 K914352
UDI-DISize and differences
CORDIS 502188
Cordis US Corp.
502188 / 50218810705032009591 —On the market
CORDIS 502190
Cordis US Corp.
502190 / 50219010705032009614 —On the market
CORDIS 502191
Cordis US Corp.
502191 / 50219110705032009621 —On the market
CORDIS 502192
Cordis US Corp.
502192 / 50219210705032009638 —On the market
CORDIS 502194
Cordis US Corp.
502194 / 50219410705032009645 —On the market

Other devices from Cordis US Corp.

See all devices from Cordis US Corp. →