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BIODERM EID MALE EXTERNAL INCONTINENCE DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963950
510(k) Type
Traditional
Applicant
BIODERM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1997
Days to Decision
100 days
Submission Type
Summary

BIODERM EID MALE EXTERNAL INCONTINENCE DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963950
510(k) Type
Traditional
Applicant
BIODERM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1997
Days to Decision
100 days
Submission Type
Summary