Plethysmograph, Volume
FDA product code JEH · 11 cleared devices
Class 2
Anesthesiology
- Regulation
- 21 CFR 868.1760
- Review panel
- AN
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1985-07-08 – 2024-12-09
JEH
2024-12-09
JEH
2023-05-25
Model 9160 VitaloQUB
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JEH
2008-04-22
MASTERSCREEN PFT, MASTERSCREEN PFT CT, MASTERSCREEN PFT BODY
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JEH
2003-01-13
BODY BOX 5500
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JEH
1997-03-28
C.E. VASCULAR MACHINE
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JEH
1995-12-12
AP-18
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JEH
1995-07-31
MASTERSCREEN PFT BODY
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JEH
1995-02-03
MASTERSCREEN BODY
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JEH
1994-01-13
EC 5R PLETHYSMOGRAPH
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JEH
1993-08-23
TELEPULSE
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JEH
1985-07-08
CYBERMEDIC CM-810 BODY PLETHYSMOGRAPH
View details →No matching devices.
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