FDA 510(k)

ANGIOGRAPHIC GUIDE WIRE

K-Number: K781561 · 1978-11-07

Decision Date1978-11-07

Product CodeDQX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

ANGIOGRAPHIC GUIDE WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Wilson Medical Instruments Co.. It received FDA 510(k) clearance on 1978-11-07 under 510(k) number K781561. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGIOGRAPHIC GUIDE WIRE?

ANGIOGRAPHIC GUIDE WIRE is a medical device that received FDA 510(k) clearance on 1978-11-07. The listed applicant is Wilson Medical Instruments Co.. The 510(k) number is K781561.

When did ANGIOGRAPHIC GUIDE WIRE receive FDA 510(k) clearance?

ANGIOGRAPHIC GUIDE WIRE received FDA 510(k) clearance on 1978-11-07, under 510(k) number K781561.

Who is the listed applicant for ANGIOGRAPHIC GUIDE WIRE?

The FDA 510(k) record lists Wilson Medical Instruments Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANGIOGRAPHIC GUIDE WIRE?

The FDA product code for ANGIOGRAPHIC GUIDE WIRE is DQX.

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Related Devices (Code: DQX)

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Official Source

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