Super Torque CP0174

by Cordis Corporation

Super Torque CP0174 is a Class II device made by Cordis Corporation, cleared under FDA 510(k) K914007 on 18 Oct 1991 and listed in FDA GUDID since 1 Aug 2016 (UDI-DI 10705032025843), 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

FDA submission, from GUDID

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10705032025843 UDI-DI	Date1 Aug 2016Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK914007	Date18 Oct 1991Decided	StatusActive

Official records

AccessGUDID record UDI-DI 10705032025843
FDA 510(k) database 510(k) number K914007

Across registries

2 registries list this device

FDA 510(k) K914007 decided 18 Oct 1991 Active
FDA GUDID UDI-DI 10705032025843 listed 1 Aug 2016 Listed

Timeline

2 dated events

18 Oct 1991 Cleared FDA 510(k) K914007
1 Aug 2016 Listed FDA GUDID 10705032025843

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Super Torque
Generic name: Angiographic catheter, single-use
Model / Ref / Catalog: CP0174

Primary DI / UDI-DI: 10705032025843
510(k) Number: K914007
FDA product code: DQO
GMDN term: Angiographic catheter, single-use

Device class: Class II
Regulation number: 870.1200
GUDID distribution status: In Commercial Distribution

Other devices from Cordis US Corp.

See all devices from Cordis US Corp. →

Properties

Supplied sterile
Single use
Prescription use
Lot / batch number
Expiration date

Other properties (10, all answered No)