NMG

Forceps, Biopsy, Gynecological, Reprocessed

Product code

NMG

Device name

Forceps, Biopsy, Gynecological, Reprocessed

Device class

Class 2

21 CFR

21 CFR 884.4530

Medical specialty

Obstetrics/Gynecology

Marketing pathway

510(K)

Flag

Third-party review eligible

FDA classification definition

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).

Definition text from the FDA device classification database (U.S. federal government work, public domain).