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Catheter, Oximeter, Fiber-Optic

FDA product code DQE · 18 cleared devices

Class 2 Cardiovascular
Regulation
21 CFR 870.1230
Review panel
CV
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1976-08-23 – 2018-02-20
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