Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA PMA

Device, thermal ablation, endometrial

PMA Number: P010013 · 2025-12-17

ApplicantHologic, Inc.
Decision Date2025-12-17
PMA NumberP010013
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 Hologic, Inc.. It received FDA 510(k) clearance on 2025-12-17. 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 2025-12-17. The listed applicant is Hologic, 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 Hologic, 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.

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.

↑