Raycell Mk2— 510(k) K161324

Name: FDA 510(k) clearance K161324
Creator: U.S. Food and Drug Administration
Published: 2016-08-12

Substantially Equivalent

Best Theratronics Limited

FDA 510(k) clearance K161324 for Raycell Mk2, Substantially Equivalent on 2016-08-12. Applicant: Best Theratronics Limited. Device class: Unclassified.

Clearance details

Applicant: Best Theratronics Limited
Product code: Code MOT
Device class: Unclassified
Advisory panel: Unknown
Date received: 2016-05-11
Decision date: 2016-08-12
Decision: Substantially Equivalent
Clearance type: Special
Location: Ottawa, CA

Download summary PDF View on FDA.gov ↗

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