Toray Industries (America), Inc.
Toray Industries (America), Inc. holds FDA 510(k) medical device clearances, first cleared 1986, most recent 2004.
Top product codes for Toray Industries (America), Inc.
Recent clearances by Toray Industries (America), Inc.
- K042370 — TORAYGUIDE GUIDEWIRE
- K030050 — TORAYSULFONE DIALYZER, BS-L SERIES
- K002512 — TORAYSULFONE DIALYZER
- K994198 — HEMOFEEL-CH, MODELS CH-0.35L, CH-0.6L, CH-1.0L
- K942681 — FILTRYZER
- K935471 — FILTRYZER(TM)
- K940910 — FILTRYZER
- K884339 — TORAY FILTRYZER DIALYZERS
- K883407 — TORAY FILTRYZER BK SERIES
- K884083 — TORAY VASCULAR PROSTHESIS
- K882158 — MODIFIED TORAY FILTRYZER DIALYZERS
- K881236 — TORAY ANTHRON P-U CATHETERS
- K874542 — TORAY SUPERSELECTIVE GUIDEWIRES, ADDITIONAL TYPES
- K872983 — TORAY ANTHRON ANGIOGRAPHIC CATHETERS
- K872762 — TORAY ANTHRON AORTA BYPASS TUBES
- K861115 — TORAY SUPERSELECTIVE GUIDEWIRE,SUPERSELEC Y-K TYPE
- K861117 — ANTHRON CATHETERS & SETS
- K861116 — TORAY ANTHRON BYPASS TUBES
Data sourced from openFDA. This site is unofficial and independent of the FDA.