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510(k) K872983

TORAY ANTHRON ANGIOGRAPHIC CATHETERS by Toray Industries (America), Inc. — Product Code DQR

K872983 is an FDA 510(k) premarket notification submitted by Toray Industries (America), Inc. for the device "TORAY ANTHRON ANGIOGRAPHIC CATHETERS". The FDA issued a decision of Substantially Equivalent on November 20, 1987. The device falls under product code DQR (Cannula, Catheter), a Class II device regulated under 21 CFR 870.1300. Toray Industries (America), Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 20, 1987
Date Received
July 31, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cannula, Catheter
Device Class
Class II
Regulation Number
870.1300
Review Panel
CV
Submission Type

Other clearances by Toray Industries (America), Inc.

  • K042370 — TORAYGUIDE GUIDEWIRE (December 17, 2004)
  • K030050 — TORAYSULFONE DIALYZER, BS-L SERIES (September 29, 2003)
  • K002512 — TORAYSULFONE DIALYZER (October 15, 2001)
  • K994198 — HEMOFEEL-CH, MODELS CH-0.35L, CH-0.6L, CH-1.0L (August 25, 2000)
  • K942681 — FILTRYZER (June 22, 1995)
  • K935471 — FILTRYZER(TM) (May 19, 1995)
  • K940910 — FILTRYZER (May 4, 1995)
  • K884339 — TORAY FILTRYZER DIALYZERS (March 17, 1989)
  • K883407 — TORAY FILTRYZER BK SERIES (February 27, 1989)
  • K884083 — TORAY VASCULAR PROSTHESIS (January 12, 1989)

Other clearances for product code DQR

  • K131446 — INTEGRA JARIT HEPARIN CANNULAS, INJECTORS, AND NEEDLES (October 28, 2013)
  • K073559 — 18 FR. RMI ARTERIAL PERFUSION CANNULA II, 20 FR. RMI ARTERIAL PERFUSION CANNULA (January 31, 2008)
  • K051655 — ANGIODYNAMICS, INC., MICRO ACCESS KITS (September 12, 2005)
  • K030398 — CARDIACASSIST TRANSSEPTAL CANNULA SET, MODEL 5132-6221 (May 23, 2003)
  • K960098 — RMI INTERNAL MAMMARY ARTERY CANNULA (March 26, 1996)
  • K902674 — DATASCOPE ARTERIAL CANNULA W/ACCESS PORT (January 16, 1991)
  • K894784 — MODIFIED SHILEY FEMORAL VENOUS CANNULA (March 28, 1990)
  • K894243 — RMI ARTERIAL PERFUSION CANNULA (September 19, 1989)
  • K884628 — HARBORIN CENTRAL VENOUS CATHETER (May 15, 1989)
  • K884478 — DAIG COLLAPSIBLE STERILE SLEEVE (February 22, 1989)

FDA data resources