FDA 510(k) Application Details - K153694

Device Classification Name	Tonometer, Manual   More FDA Info for this Device
510(K) Number	K153694
Device Name	Tonometer, Manual
Applicant	Icare Finland Oy Ayritie 22 Vantaa FI-01510 FI Other 510(k) Applications for this Company
Contact	Matti Tulikoura Other 510(k) Applications for this Contact
Regulation Number	886.1930   More FDA Info for this Regulation Number
Classification Product Code	HKY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/23/2015
Decision Date	04/19/2016
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OP - Ophthalmic
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review