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FDA 510(k)

ASAHI ANGIOGRAPHIC CATHETER

K-Number: K051561 · 2005-11-02

ApplicantAsahi Intecc Co., Ltd.
Decision Date2005-11-02
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ASAHI ANGIOGRAPHIC CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Asahi Intecc Co., Ltd.. It received FDA 510(k) clearance on 2005-11-02 under 510(k) number K051561. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASAHI ANGIOGRAPHIC CATHETER?

ASAHI ANGIOGRAPHIC CATHETER is a medical device that received FDA 510(k) clearance on 2005-11-02. The listed applicant is Asahi Intecc Co., Ltd.. The 510(k) number is K051561.

When did ASAHI ANGIOGRAPHIC CATHETER receive FDA 510(k) clearance?

ASAHI ANGIOGRAPHIC CATHETER received FDA 510(k) clearance on 2005-11-02, under 510(k) number K051561.

Who is the listed applicant for ASAHI ANGIOGRAPHIC CATHETER?

The FDA 510(k) record lists Asahi Intecc Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ASAHI ANGIOGRAPHIC CATHETER?

The FDA product code for ASAHI ANGIOGRAPHIC CATHETER is DQO.

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Related Devices (Code: DQO)

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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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