FDA 510(k), K941507, THEMO-FLO SYSTEM 3 LAPAROSCOPIC/HYSTEROSCOPIC SYSTEM
FDA 510(k), K941507, THEMO-FLO SYSTEM 3 LAPAROSCOPIC/HYSTEROSCOPIC SYSTEM
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510(K) Number: K941507
Device Name: THEMO-FLO SYSTEM 3 LAPAROSCOPIC/HYSTEROSCOPIC SYSTEM
Manufacturer:
Device Classification Name: Laparoscope, Gynecologic (And Accessories)
Regulation Number: 884.1720
Classification Product Code: HET
Date Received: 03/29/1994
Decision Date: 03/06/1995
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: THEMO-FLO SYSTEM 3 LAPAROSCOPIC/HYSTEROSCOPIC SYSTEM
Manufacturer:
Device Classification Name: Laparoscope, Gynecologic (And Accessories)
Regulation Number: 884.1720
Classification Product Code: HET
Date Received: 03/29/1994
Decision Date: 03/06/1995
Regulation Medical Specialty: Obstetrics/Gynecology