• FDA 510(k) records for MobileRay Pulse SE Digital Imaging System K191503
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FDA 510(k) K111170, PICO, by Smith & Nephew, Inc.

FDA 510(k) K111170, PICO, by Smith & Nephew, Inc.

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510(K) Number: K111170
Device Name: PICO
Manufacturer: Smith & Nephew, Inc.
Device Classification Name: negative pressure wound therapy powered suction pump
Regulation Number: 878.4780
Classification Product Code: OMP
Date Received: 04/26/2011
Decision Date: 12/15/2011
Regulation Medical Specialty: General & Plastic Surgery
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