FDA 510(k)

MICROVASIVE INJECTION GOLD PROBE

K-Number: K942301 · 1994-11-02

Decision Date1994-11-02

Product CodeKNS

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

MICROVASIVE INJECTION GOLD PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 1994-11-02 under 510(k) number K942301. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROVASIVE INJECTION GOLD PROBE?

MICROVASIVE INJECTION GOLD PROBE is a medical device that received FDA 510(k) clearance on 1994-11-02. The listed applicant is Boston Scientific Corp. The 510(k) number is K942301.

When did MICROVASIVE INJECTION GOLD PROBE receive FDA 510(k) clearance?

MICROVASIVE INJECTION GOLD PROBE received FDA 510(k) clearance on 1994-11-02, under 510(k) number K942301.

Who is the listed applicant for MICROVASIVE INJECTION GOLD PROBE?

The FDA 510(k) record lists Boston Scientific Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROVASIVE INJECTION GOLD PROBE?

The FDA product code for MICROVASIVE INJECTION GOLD PROBE is KNS.

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Related Devices (Code: KNS)

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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.