Medical Device Manufacturer · US , New York , NY

Toray Industries (America), Inc. - FDA 510(k) Cleared Devices

18 submissions · 18 cleared · Since 1986

18

Total

18

Cleared

0

Denied

FDA 510(k) Regulatory Record - Toray Industries (America), Inc. Cardiovascular ✕

7 devices

1-7 of 7

Cleared Dec 17, 2004

TORAYGUIDE GUIDEWIRE

Cardiovascular · 108d

Cleared Jan 12, 1989

TORAY VASCULAR PROSTHESIS

Cardiovascular · 107d

Cleared Mar 07, 1988

TORAY SUPERSELECTIVE GUIDEWIRES, ADDITIONAL TYPES

Cardiovascular · 125d

Cleared Nov 20, 1987

TORAY ANTHRON ANGIOGRAPHIC CATHETERS

Cardiovascular · 112d

Cleared Sep 24, 1987

TORAY ANTHRON AORTA BYPASS TUBES

Cardiovascular · 73d

Cleared Jul 11, 1986

TORAY SUPERSELECTIVE GUIDEWIRE,SUPERSELEC Y-K TYPE

Cardiovascular · 108d

Cleared May 28, 1986

TORAY ANTHRON BYPASS TUBES

Cardiovascular · 64d