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Catheter, Retention Type

FDA product code EZK · 3 cleared devices

Class 2 Gastroenterology, Urology
Regulation
21 CFR 876.5980
Review panel
GU
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1977-03-15 – 1992-11-16
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