CRYOTRON 2 CRYOTHERAPY DEVICE— 510(k) K030281

Name: FDA 510(k) clearance K030281
Creator: U.S. Food and Drug Administration
Published: 2003-08-20

Substantially Equivalent

Cryonic Medical North America

FDA 510(k) clearance K030281 for CRYOTRON 2 CRYOTHERAPY DEVICE, Substantially Equivalent on 2003-08-20. Applicant: Cryonic Medical North America. Device class: Unclassified.

Clearance details

Applicant: Cryonic Medical North America
Product code: Code MLY
Device class: Unclassified
Advisory panel: Unknown
Date received: 2003-01-27
Decision date: 2003-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montecito, 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.