FES
1989-05-30
Recorder, External, Pressure, Amplifier & Transducer
FDA product code FES · 2 cleared devices
Class 2
Gastroenterology, Urology
- Regulation
- 21 CFR 876.1725
- Review panel
- GU
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1980-08-27 – 1989-05-30
FES
1980-08-27
MMI/GAELTEC CATHETER TIP PRESS. TRANSDU
View details →No matching devices.
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