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Forceps, Biopsy, Non-Electric, Reprocessed

FDA product code NON · 3 cleared devices

Class 1 Gastroenterology, Urology
Regulation
21 CFR 876.1075
Review panel
GU
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
2005-01-25 – 2005-07-20

same as procode FCL except this product is for the reprocessed device. Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).

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