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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name anomaloscope
510(k) Number K930575
Device Name KAMPPETER ANOMALOSCOPE
Applicant
BOVA INTL.
2217 SIXTH AVE.
FORT WORTH,  TX  76116
Applicant Contact BODO OEHLER
Correspondent
BOVA INTL.
2217 SIXTH AVE.
FORT WORTH,  TX  76116
Correspondent Contact BODO OEHLER
Regulation Number886.1070
Classification Product Code
HIW  
Date Received02/04/1993
Decision Date 02/25/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
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