SYNTHEMED DEVICE— 510(k) K082276

Substantially Equivalent

Synthemed, Inc.

FDA 510(k) clearance K082276 for SYNTHEMED DEVICE, Substantially Equivalent on 2008-11-18. Applicant: Synthemed, Inc..

Clearance details

Applicant: Synthemed, Inc.
Product code: Code LYA
Advisory panel: Ear, Nose, Throat
Date received: 2008-08-11
Decision date: 2008-11-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Iselin, NJ, US

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