Last synced on 14 November 2025 at 11:06 pm

Rapid Reboot Compression Therapy System

Page Type
Cleared 510(K)
510(k) Number
K182668
510(k) Type
Traditional
Applicant
Rapid Reboot Recovery Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2018
Days to Decision
80 days
Submission Type
Summary

Rapid Reboot Compression Therapy System

Page Type
Cleared 510(K)
510(k) Number
K182668
510(k) Type
Traditional
Applicant
Rapid Reboot Recovery Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2018
Days to Decision
80 days
Submission Type
Summary