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CARDIOSLEEVE

Page Type
Cleared 510(K)
510(k) Number
K131287
510(k) Type
Traditional
Applicant
RIJUVEN CORP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/2013
Days to Decision
49 days
Submission Type
Summary

CARDIOSLEEVE

Page Type
Cleared 510(K)
510(k) Number
K131287
510(k) Type
Traditional
Applicant
RIJUVEN CORP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/2013
Days to Decision
49 days
Submission Type
Summary