Rapid Reboot Compression Therapy System— 510(k) K182668

Name: FDA 510(k) clearance K182668
Creator: U.S. Food and Drug Administration
Published: 2018-12-14

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. Device class: 2.

Clearance details

Applicant: Rapid Reboot Recovery Products, LLC
Product code: Code IRP
Device class: Class 2
Regulation: 21 CFR 890.5650
Advisory panel: Physical Medicine
Date received: 2018-09-25
Decision date: 2018-12-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lindon, UT, 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.