Rapid Reboot Compression Therapy System— 510(k) K182668

Substantially Equivalent

Rapid Reboot Recovery Products, LLC

FDA 510(k) clearance K182668 for Rapid Reboot Compression Therapy System, Substantially Equivalent on 2018-12-14. Applicant: Rapid Reboot Recovery Products, LLC.

Clearance details

Applicant: Rapid Reboot Recovery Products, LLC
Product code: Code IRP
Advisory panel: Physical Medicine
Date received: 2018-09-25
Decision date: 2018-12-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lindon, UT, US

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