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FDA 510(k)

PRECIOUS PLUS GUIDE CATHETER

K-Number: K072316 · 2007-09-17

ApplicantAsahi Intecc Co., Ltd.
Decision Date2007-09-17
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PRECIOUS PLUS GUIDE 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 2007-09-17 under 510(k) number K072316. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRECIOUS PLUS GUIDE CATHETER?

PRECIOUS PLUS GUIDE CATHETER is a medical device that received FDA 510(k) clearance on 2007-09-17. The listed applicant is Asahi Intecc Co., Ltd.. The 510(k) number is K072316.

When did PRECIOUS PLUS GUIDE CATHETER receive FDA 510(k) clearance?

PRECIOUS PLUS GUIDE CATHETER received FDA 510(k) clearance on 2007-09-17, under 510(k) number K072316.

Who is the listed applicant for PRECIOUS PLUS GUIDE 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 PRECIOUS PLUS GUIDE CATHETER?

The FDA product code for PRECIOUS PLUS GUIDE CATHETER is DQY.

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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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