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BIODERM EID MALE EXTERNAL INCONTINENCE DEVICE

Page Type
Cleared 510(K)
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)
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