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INTERMED ZOOM COLPOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K031639
510(k) Type
Traditional
Applicant
INTERMED GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2003
Days to Decision
87 days
Submission Type
Summary

INTERMED ZOOM COLPOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K031639
510(k) Type
Traditional
Applicant
INTERMED GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2003
Days to Decision
87 days
Submission Type
Summary