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Alliance gains the US nod for more reprocessed products:

This article was originally published in Clinica

Executive Summary

Alliance Medical has received three more US FDA 510(k) clearances for reprocessed medical devices. The FDA has now approved 15 of the 20 510(k) applications filed by the Phoenix, Arizona firm. Reprocessed devices covered by the latest clearances include hot biopsy forceps, laparoscopic/endoscopic instruments and polypectomy snares.

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