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Needle, Biopsy, Cardiovascular

FDA product code DWO · 11 cleared devices

Class 1 General, Plastic Surgery
Regulation
21 CFR 878.4800
Review panel
SU
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1982-03-23 – 1994-02-15
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