FDA 510(k) Application Details - K101141

Device Classification Name	Colposcope (And Colpomicroscope)   More FDA Info for this Device
510(K) Number	K101141
Device Name	Colposcope (And Colpomicroscope)
Applicant	SEILER PRECISION MICROSCOPES 3433 TREE CT INDUSTRIAL BLVD ST. LOUIS, MO 63122 US Other 510(k) Applications for this Company
Contact	DAN MEYER Other 510(k) Applications for this Contact
Regulation Number	884.1630   More FDA Info for this Regulation Number
Classification Product Code	HEX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/22/2010
Decision Date	08/06/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review