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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Esthesiometer, Ocular
510(k) Number K920271
Device Name WEINSTEIN CORNEAL MIRCOAESTHESIOMETER
Applicant
Connecticut Bioinstruments, Inc.
5 B Oak Ln.
Danbury,  CT  06811
Applicant Contact CURT WEINSTEIN
Correspondent
Connecticut Bioinstruments, Inc.
5 B Oak Ln.
Danbury,  CT  06811
Correspondent Contact CURT WEINSTEIN
Regulation Number886.1040
Classification Product Code
HJC  
Date Received01/22/1992
Decision Date 04/21/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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