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DIOSCAN

Page Type
Cleared 510(K)
510(k) Number
K990014
510(k) Type
Traditional
Applicant
DIOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1999
Days to Decision
53 days
Submission Type
Summary

DIOSCAN

Page Type
Cleared 510(K)
510(k) Number
K990014
510(k) Type
Traditional
Applicant
DIOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1999
Days to Decision
53 days
Submission Type
Summary