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Alliger Ultrasonic Surgical System

by Medsonic, Inc.

510(k) K933559

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

1 closed

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK933559 Date15 Oct 1993ClearedStatusActive

Recalls

1 recall · FDA

    • Terminated Z-0070-04 FDA Unclassified (pre-2012) initiated 13 Aug 2003

    Firm received complaints of tingling or static shock sensation to end users caused by forcing the output connector into its receptacle misaligned. The misalignment causes additional voltage to appear on the patient probe.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
LFL
Device Class
U
Advisory Committee
Unknown
FDA Decision
SESE Substantially Equivalent