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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name tonometer, ac-powered
510(k) Number K884012
Device Name MMAC II TONOMETER
Applicant
PROFESSIONAL TECHNOLOGIES CORP.
P.O. BOX 932
REDDING,  CA  96099
Applicant Contact SCHWALBE, JR.
Correspondent
PROFESSIONAL TECHNOLOGIES CORP.
P.O. BOX 932
REDDING,  CA  96099
Correspondent Contact SCHWALBE, JR.
Regulation Number886.1930
Classification Product Code
HKX  
Date Received09/22/1988
Decision Date 01/06/1989
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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