Last synced on 25 April 2025 at 11:05 pm

HANDI-FOAM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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