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FDA 510(k)

KCK INDUSTRIES' SURGICAL INSTRUMENTS

K-Number: K871894 · 1987-06-23

ApplicantKck Industries
Decision Date1987-06-23
Product CodeGDX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KCK INDUSTRIES' SURGICAL INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Kck Industries. It received FDA 510(k) clearance on 1987-06-23 under 510(k) number K871894. The device is classified under product code GDX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KCK INDUSTRIES' SURGICAL INSTRUMENTS?

KCK INDUSTRIES' SURGICAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1987-06-23. The listed applicant is Kck Industries. The 510(k) number is K871894.

When did KCK INDUSTRIES' SURGICAL INSTRUMENTS receive FDA 510(k) clearance?

KCK INDUSTRIES' SURGICAL INSTRUMENTS received FDA 510(k) clearance on 1987-06-23, under 510(k) number K871894.

Who is the listed applicant for KCK INDUSTRIES' SURGICAL INSTRUMENTS?

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

What is the FDA product code for KCK INDUSTRIES' SURGICAL INSTRUMENTS?

The FDA product code for KCK INDUSTRIES' SURGICAL INSTRUMENTS is GDX.

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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.

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