CRYO-TOUCH III— 510(k) K120415

Substantially Equivalent

Myoscience, Inc.

FDA 510(k) clearance K120415 for CRYO-TOUCH III, Substantially Equivalent on 2012-06-22. Applicant: Myoscience, Inc.. Device class: 2.

Clearance details

Applicant: Myoscience, Inc.
Product code: Code GXH
Device class: Class 2
Regulation: 21 CFR 882.4250
Advisory panel: Neurology
Date received: 2012-02-10
Decision date: 2012-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Redwood City, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.