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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Computer, Diagnostic, Programmable
510(k) Number K912728
Device Name ALTAIR
Applicant
Diagnostic Medical Instruments
6724 Thompson Rd.
Syracuse,  NY  13211
Applicant Contact FREDERICK V CANNITO
Correspondent
Diagnostic Medical Instruments
6724 Thompson Rd.
Syracuse,  NY  13211
Correspondent Contact FREDERICK V CANNITO
Regulation Number870.1425
Classification Product Code
DQK  
Date Received06/20/1991
Decision Date 02/27/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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