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HANDI-FOAM

Page Type
Cleared 510(K)
510(k) Number
K935021
510(k) Type
Traditional
Applicant
MEDTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/1994
Days to Decision
169 days
Submission Type
Statement

HANDI-FOAM

Page Type
Cleared 510(K)
510(k) Number
K935021
510(k) Type
Traditional
Applicant
MEDTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/1994
Days to Decision
169 days
Submission Type
Statement