FDA 510(k), K950339, KSEA STEINER ELECTROMECHANIC MORCELLATOR
FDA 510(k), K950339, KSEA STEINER ELECTROMECHANIC MORCELLATOR
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$149.00 USD
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510(K) Number: K950339
Device Name: KSEA STEINER ELECTROMECHANIC MORCELLATOR
Manufacturer:
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 01/27/1995
Decision Date: 04/06/1995
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: KSEA STEINER ELECTROMECHANIC MORCELLATOR
Manufacturer:
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 01/27/1995
Decision Date: 04/06/1995
Regulation Medical Specialty: Gastroenterology/Urology