CryoVizion System— 510(k) K183485

Name: FDA 510(k) clearance K183485
Creator: U.S. Food and Drug Administration
Published: 2019-08-28

Substantially Equivalent

Cryos Technologies, Inc.

FDA 510(k) clearance K183485 for CryoVizion System, Substantially Equivalent on 2019-08-28. Applicant: Cryos Technologies, Inc.. Device class: Unclassified.

Clearance details

Applicant: Cryos Technologies, Inc.
Product code: Code LDK
Device class: Unclassified
Advisory panel: Unknown
Date received: 2018-12-17
Decision date: 2019-08-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Joliette, CA

Download summary PDF View on FDA.gov ↗

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