Raycell MK1— 510(k) K181737

Name: FDA 510(k) clearance K181737
Creator: U.S. Food and Drug Administration
Published: 2019-01-02

Substantially Equivalent

Best Theratronics Limited

FDA 510(k) clearance K181737 for Raycell MK1, Substantially Equivalent on 2019-01-02. 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: 2018-07-02
Decision date: 2019-01-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ottawa, CA

Download summary PDF View on FDA.gov ↗

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