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Actuator, Syringe, Injector Type

FDA product code DQF · 3 cleared devices

Class 2 Cardiovascular
Regulation
21 CFR 870.1670
Review panel
HO
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1988-03-22 – 1992-07-13
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