Product code NON

Device name

Forceps, Biopsy, Non-Electric, Reprocessed

Medical specialty

Gastroenterology, Urology

Device class

1

Regulation number

876.1075

Review panel

GU

Implant

N

Life sustaining/supporting

N

GMP exempt

N

Third party review

Y

Summary malfunction reporting

Eligible

Definition

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).

Source

FDA openFDA device classification dataset