Last synced on 17 May 2024 at 11:06 pm

ECLERIS MICROSTAR COLPOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100595
510(k) Type
Traditional
Applicant
Ecleris USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/2010
Days to Decision
129 days
Submission Type
Statement

ECLERIS MICROSTAR COLPOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100595
510(k) Type
Traditional
Applicant
Ecleris USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/2010
Days to Decision
129 days
Submission Type
Statement