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Microsulis Microwave Endometrial Ablation (MEA) System

by Microsulis Medical, Ltd.

PMA P020031

Withdrawn Withdrawn in United States.

Was authorized under PMA, withdrawn

Ended

Withdrawn 23 Sep 2003

PMA

FDA recalls

None found

in data synced 6 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA PMA, synced 6 Oct 2026. What this means

Regulatory status

as of registry sync 6 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA PMAAPWD Approval withdrawn NumberP020031 Date23 Sep 2003Approval withdrawnStatusWithdrawn

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 6 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA PMA Withdrawn

Specification

PMA

Full name
Microsulis Microwave Endometerial Ablation (Mea) System
Trade Name
Microsulis Microwave Endometrial Ablation (Mea) System
Generic Name
Device, thermal ablation, endometrial
FDA applicant
Microsulis Medical , Ltd.
PMA Number
FDA Product Code
MNB
Device Class
Class III
Advisory Committee
Obstetrics/Gynecology
FDA Decision
APWD Approval withdrawn

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