INTERMED ZOOM COLPOSCOPE— 510(k) K031639

Substantially Equivalent

Intermed Group, Inc.

FDA 510(k) clearance K031639 for INTERMED ZOOM COLPOSCOPE, Substantially Equivalent on 2003-08-22. Applicant: Intermed Group, Inc..

Clearance details

Applicant: Intermed Group, Inc.
Product code: Code HEX
Advisory panel: Obstetrics/Gynecology
Date received: 2003-05-27
Decision date: 2003-08-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Worth, FL, US

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