Reprocessed Cordless Ultrasonic Dissection Device— 510(k) K143562

Substantially Equivalent

Sterilmed, Inc.

FDA 510(k) clearance K143562 for Reprocessed Cordless Ultrasonic Dissection Device, Substantially Equivalent on 2015-05-20. Applicant: Sterilmed, Inc..

Clearance details

Applicant: Sterilmed, Inc.
Product code: Code NLQ
Advisory panel: Unknown
Date received: 2014-12-16
Decision date: 2015-05-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Maple Grove, MN, US

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