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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stethoscope, Manual
510(k) Number K854771
Device Name SALTZMAN STETHOSCOPE HEAD
Applicant
K & S Medicorp
7860 SW 147 St.
Miami,  FL  33158
Applicant Contact SALTZMAN MD
Correspondent
K & S Medicorp
7860 SW 147 St.
Miami,  FL  33158
Correspondent Contact SALTZMAN MD
Regulation Number870.1875
Classification Product Code
LDE  
Date Received11/29/1985
Decision Date 05/09/1986
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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