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FDA 510(k)

DUAL INCISION TUBAL OCCLUS. BAND APPLI.

K-Number: K771961 · 1977-10-25

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

Device Summary

DUAL INCISION TUBAL OCCLUS. BAND APPLI. 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 K771961. 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 DUAL INCISION TUBAL OCCLUS. BAND APPLI.?

DUAL INCISION TUBAL OCCLUS. BAND APPLI. is a medical device that received FDA 510(k) clearance on 1977-10-25. The listed applicant is Kli. The 510(k) number is K771961.

When did DUAL INCISION TUBAL OCCLUS. BAND APPLI. receive FDA 510(k) clearance?

DUAL INCISION TUBAL OCCLUS. BAND APPLI. received FDA 510(k) clearance on 1977-10-25, under 510(k) number K771961.

Who is the listed applicant for DUAL INCISION TUBAL OCCLUS. BAND APPLI.?

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 DUAL INCISION TUBAL OCCLUS. BAND APPLI.?

The FDA product code for DUAL INCISION TUBAL OCCLUS. BAND APPLI. 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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