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FDA 510(k)

TUBAL OCCLUSION INSERTER/LAPAROSCOPE

K-Number: K771960 · 1977-10-25

ApplicantKli
Decision Date1977-10-25
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TUBAL OCCLUSION INSERTER/LAPAROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Kli. It received FDA 510(k) clearance on 1977-10-25 under 510(k) number K771960. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBAL OCCLUSION INSERTER/LAPAROSCOPE?

TUBAL OCCLUSION INSERTER/LAPAROSCOPE is a medical device that received FDA 510(k) clearance on 1977-10-25. The listed applicant is Kli. The 510(k) number is K771960.

When did TUBAL OCCLUSION INSERTER/LAPAROSCOPE receive FDA 510(k) clearance?

TUBAL OCCLUSION INSERTER/LAPAROSCOPE received FDA 510(k) clearance on 1977-10-25, under 510(k) number K771960.

Who is the listed applicant for TUBAL OCCLUSION INSERTER/LAPAROSCOPE?

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

What is the FDA product code for TUBAL OCCLUSION INSERTER/LAPAROSCOPE?

The FDA product code for TUBAL OCCLUSION INSERTER/LAPAROSCOPE is HET.

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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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