FDA 510(k), K133314, HARMONIC FOCUS SHEARS + ADAPTIVE TISSUE TECHNOLOGY
FDA 510(k), K133314, HARMONIC FOCUS SHEARS + ADAPTIVE TISSUE TECHNOLOGY
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510(K) Number: K133314
Device Name: HARMONIC FOCUS SHEARS + ADAPTIVE TISSUE TECHNOLOGY
Manufacturer:
Device Classification Name: Instrument, Ultrasonic Surgical
Regulation Number:
Classification Product Code: LFL
Date Received: 10/28/2013
Decision Date: 12/03/2013
Regulation Medical Specialty:
Device Name: HARMONIC FOCUS SHEARS + ADAPTIVE TISSUE TECHNOLOGY
Manufacturer:
Device Classification Name: Instrument, Ultrasonic Surgical
Regulation Number:
Classification Product Code: LFL
Date Received: 10/28/2013
Decision Date: 12/03/2013
Regulation Medical Specialty: