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LEICA COLPOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000707
510(k) Type
Traditional
Applicant
LEICA MICROSCOPY SYSTEMS LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/2000
Days to Decision
117 days
Submission Type
Summary

LEICA COLPOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000707
510(k) Type
Traditional
Applicant
LEICA MICROSCOPY SYSTEMS LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/2000
Days to Decision
117 days
Submission Type
Summary