Last synced on 14 November 2025 at 11:06 pm

DIAPEX

Page Type
Cleared 510(K)
510(k) Number
K033585
510(k) Type
Traditional
Applicant
BISCO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/2004
Days to Decision
64 days
Submission Type
Summary

DIAPEX

Page Type
Cleared 510(K)
510(k) Number
K033585
510(k) Type
Traditional
Applicant
BISCO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/2004
Days to Decision
64 days
Submission Type
Summary