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FDA 510(k)

TORAY ANTHRON ANGIOGRAPHIC CATHETERS

K-Number: K872983 · 1987-11-20

ApplicantToray Industries (America), Inc.
Decision Date1987-11-20
Product CodeDQR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TORAY ANTHRON ANGIOGRAPHIC CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Toray Industries (America), Inc.. It received FDA 510(k) clearance on 1987-11-20 under 510(k) number K872983. The device is classified under product code DQR. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TORAY ANTHRON ANGIOGRAPHIC CATHETERS?

TORAY ANTHRON ANGIOGRAPHIC CATHETERS is a medical device that received FDA 510(k) clearance on 1987-11-20. The listed applicant is Toray Industries (America), Inc.. The 510(k) number is K872983.

When did TORAY ANTHRON ANGIOGRAPHIC CATHETERS receive FDA 510(k) clearance?

TORAY ANTHRON ANGIOGRAPHIC CATHETERS received FDA 510(k) clearance on 1987-11-20, under 510(k) number K872983.

Who is the listed applicant for TORAY ANTHRON ANGIOGRAPHIC CATHETERS?

The FDA 510(k) record lists Toray Industries (America), Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TORAY ANTHRON ANGIOGRAPHIC CATHETERS?

The FDA product code for TORAY ANTHRON ANGIOGRAPHIC CATHETERS is DQR.

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Other records listing Toray Industries (America), Inc. as applicant

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Related Devices (Code: DQR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K131446INTEGRA JARIT HEPARIN CANNULAS, INJECTORS, AND NEEDLESIntegra LifeSciences CorporationK07355918 FR. RMI ARTERIAL PERFUSION CANNULA II, 20 FR. RMI ARTERIAL PERFUSION CANNULA IIEdwards Lifesciences Research MedicalK051655ANGIODYNAMICS, INC., MICRO ACCESS KITSAngioDynamics, Inc.K030398CARDIACASSIST TRANSSEPTAL CANNULA SET, MODEL 5132-6221Cardiacassist, Inc.K960098RMI INTERNAL MAMMARY ARTERY CANNULAResearch Medical, Inc.K902674DATASCOPE ARTERIAL CANNULA W/ACCESS PORTDatascope Corp.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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