Last synced on 4 February 2023 at 10:33 pm

INTERMED ZOOM COLPOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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