HEP
2010-08-10
Monitor, Blood-Flow, Ultrasonic
FDA product code HEP · 4 cleared devices
Class 2
Obstetrics/Gynecology
- Regulation
- 21 CFR 884.2660
- Review panel
- OB
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1991-06-24 – 2010-08-10
HEP
2003-03-03
BABYCARE
View details →
HEP
1992-09-15
ULTRACELL INSTRUMENT WIPE
View details →
HEP
1991-06-24
POCKET DOP 3
View details →No matching devices.
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