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FDA PMA

Device, thermal ablation, endometrial

PMA Number: P000032 · 2018-07-11

ApplicantCooperSurgical, Inc.
Decision Date2018-07-11
PMA NumberP000032
Product CodeMNB
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeOB

Device Summary

Device, thermal ablation, endometrial is the device name listed in this FDA 510(k) record. The listed applicant is CooperSurgical, Inc.. It received FDA 510(k) clearance on 2018-07-11. The device is classified under product code MNB. It was reviewed by the OB advisory panel.

Frequently Asked Questions

What is the Device, thermal ablation, endometrial?

Device, thermal ablation, endometrial is a medical device that received FDA 510(k) clearance on 2018-07-11. The listed applicant is CooperSurgical, Inc..

When did Device, thermal ablation, endometrial receive FDA 510(k) clearance?

The clearance date for Device, thermal ablation, endometrial can be found in the official FDA records.

Who is the listed applicant for Device, thermal ablation, endometrial?

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

What is the FDA product code for Device, thermal ablation, endometrial?

The FDA product code for Device, thermal ablation, endometrial is MNB.

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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