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FDA 510(k)

SINGLE INCISION TUBAL OCCLU. BAND APPL.

K-Number: K771963 · 1977-10-25

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

Device Summary

SINGLE INCISION TUBAL OCCLU. BAND APPL. 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 K771963. 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 SINGLE INCISION TUBAL OCCLU. BAND APPL.?

SINGLE INCISION TUBAL OCCLU. BAND APPL. is a medical device that received FDA 510(k) clearance on 1977-10-25. The listed applicant is Kli. The 510(k) number is K771963.

When did SINGLE INCISION TUBAL OCCLU. BAND APPL. receive FDA 510(k) clearance?

SINGLE INCISION TUBAL OCCLU. BAND APPL. received FDA 510(k) clearance on 1977-10-25, under 510(k) number K771963.

Who is the listed applicant for SINGLE INCISION TUBAL OCCLU. BAND APPL.?

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 SINGLE INCISION TUBAL OCCLU. BAND APPL.?

The FDA product code for SINGLE INCISION TUBAL OCCLU. BAND APPL. 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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