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FDA 510(k)

K AND D HOME TRACT

K-Number: K872121 · 1987-08-12

ApplicantJoseph A. Kott, M.D.
Decision Date1987-08-12
Product CodeHST
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

K AND D HOME TRACT is the device name listed in this FDA 510(k) record. The listed applicant is Joseph A. Kott, M.D.. It received FDA 510(k) clearance on 1987-08-12 under 510(k) number K872121. The device is classified under product code HST. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the K AND D HOME TRACT?

K AND D HOME TRACT is a medical device that received FDA 510(k) clearance on 1987-08-12. The listed applicant is Joseph A. Kott, M.D.. The 510(k) number is K872121.

When did K AND D HOME TRACT receive FDA 510(k) clearance?

K AND D HOME TRACT received FDA 510(k) clearance on 1987-08-12, under 510(k) number K872121.

Who is the listed applicant for K AND D HOME TRACT?

The FDA 510(k) record lists Joseph A. Kott, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for K AND D HOME TRACT?

The FDA product code for K AND D HOME TRACT is HST.

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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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