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Dilator, Esophageal

FDA product code KNQ · 40 cleared devices

Class 2 Gastroenterology, Urology
Regulation
21 CFR 876.5365
Review panel
GU
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1981-09-01 – 2012-10-24
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