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VIBROFLEX

Page Type
Cleared 510(K)
510(k) Number
K863197
510(k) Type
Traditional
Applicant
STOFFREGEN & CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/1986
Days to Decision
31 days

VIBROFLEX

Page Type
Cleared 510(K)
510(k) Number
K863197
510(k) Type
Traditional
Applicant
STOFFREGEN & CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/1986
Days to Decision
31 days