HEK
2006-04-10
Monitor, Heart Sound, Fetal, Ultrasonic
FDA product code HEK · 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
- 1977-07-14 – 2006-04-10
HEK
1990-10-22
FETAL PULSE DETECTOR MODEL DOP-1
View details →
HEK
1988-12-15
BIODOP(TM)
View details →
HEK
1977-07-14
DOPPLER (UTD-5 & UTD-6)
View details →No matching devices.
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