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FDA PMA

Laparoscopic contraceptive tubal occlusion device

PMA Number: P870076 · 2021-05-19

ApplicantGyrus Acmi, Inc.
Decision Date2021-05-19
PMA NumberP870076
Product CodeKNH
Device ClassClass 3
Medical SpecialtyO
Regulation Number21 CFR 8
Advisory CommitteeOB

Device Summary

Laparoscopic contraceptive tubal occlusion device is the device name listed in this FDA 510(k) record. The listed applicant is Gyrus Acmi, Inc.. It received FDA 510(k) clearance on 2021-05-19. The device is classified under product code KNH. It was reviewed by the OB advisory panel.

Frequently Asked Questions

What is the Laparoscopic contraceptive tubal occlusion device?

Laparoscopic contraceptive tubal occlusion device is a medical device that received FDA 510(k) clearance on 2021-05-19. The listed applicant is Gyrus Acmi, Inc..

When did Laparoscopic contraceptive tubal occlusion device receive FDA 510(k) clearance?

The clearance date for Laparoscopic contraceptive tubal occlusion device can be found in the official FDA records.

Who is the listed applicant for Laparoscopic contraceptive tubal occlusion device?

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

What is the FDA product code for Laparoscopic contraceptive tubal occlusion device?

The FDA product code for Laparoscopic contraceptive tubal occlusion device is KNH.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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