FDA Product Code NON: Forceps, Biopsy, Non-electric, Reprocessed

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).

Leading manufacturers include Vanguard Medical Concepts, Inc. and Sterilmed, Inc..