FDA 510(k), K946147, KSE STEINER ELECTROMECHANIC MORCELLATOR

FDA 510(k), K946147, KSE STEINER ELECTROMECHANIC MORCELLATOR

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510(K) Number: K946147
Device Name: KSE STEINER ELECTROMECHANIC MORCELLATOR
Manufacturer:
Device Classification Name: Laparoscope, Gynecologic (And Accessories)
Regulation Number: 884.1720
Classification Product Code: HET
Date Received: 12/16/1994
Decision Date: 05/25/1995
Regulation Medical Specialty: Obstetrics/Gynecology
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