FDA 510(k), K091135, RUTTER SUPRA STOMAL STENTS

FDA 510(k), K091135, RUTTER SUPRA STOMAL STENTS

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510(K) Number: K091135
Device Name: RUTTER SUPRA STOMAL STENTS
Manufacturer:
Device Classification Name: Prosthesis, Larynx (Stents And Keels)
Regulation Number: 874.3620
Classification Product Code: FWN
Date Received: 04/20/2009
Decision Date: 09/14/2009
Regulation Medical Specialty: Ear Nose & Throat
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