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FDA 510(k)

DRAPE, MICROSCOPE

K-Number: K792176 · 1979-12-10

ApplicantChris Co., Inc.
Decision Date1979-12-10
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DRAPE, MICROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Chris Co., Inc.. It received FDA 510(k) clearance on 1979-12-10 under 510(k) number K792176. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRAPE, MICROSCOPE?

DRAPE, MICROSCOPE is a medical device that received FDA 510(k) clearance on 1979-12-10. The listed applicant is Chris Co., Inc.. The 510(k) number is K792176.

When did DRAPE, MICROSCOPE receive FDA 510(k) clearance?

DRAPE, MICROSCOPE received FDA 510(k) clearance on 1979-12-10, under 510(k) number K792176.

Who is the listed applicant for DRAPE, MICROSCOPE?

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

What is the FDA product code for DRAPE, MICROSCOPE?

The FDA product code for DRAPE, MICROSCOPE is KKX.

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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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