TRANSONIC TISSUE PERFUSION MONITOR— 510(k) K140740

Substantially Equivalent

Transonic Systems, Inc.

FDA 510(k) clearance K140740 for TRANSONIC TISSUE PERFUSION MONITOR, Substantially Equivalent on 2015-07-23. Applicant: Transonic Systems, Inc..

Clearance details

Applicant: Transonic Systems, Inc.
Product code: Code DPW
Advisory panel: Cardiovascular
Date received: 2014-03-25
Decision date: 2015-07-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ithaca, NY, US

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