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MASSATOR-PEDIO

Page Type
Cleared 510(K)
510(k) Number
K833840
510(k) Type
Traditional
Applicant
TRILEEN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/1983
Days to Decision
26 days

MASSATOR-PEDIO

Page Type
Cleared 510(K)
510(k) Number
K833840
510(k) Type
Traditional
Applicant
TRILEEN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/1983
Days to Decision
26 days