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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
510(k) Number K925424
Device Name MEDICAL MANUFACTURING INC GAS SAMPLING LINES&CONN.
Applicant
Medical Manufacturers, Inc.
1290 Sanchez St.
Suite #2
San Francisco,  CA  94114
Applicant Contact DENNIS REAGER
Correspondent
Medical Manufacturers, Inc.
1290 Sanchez St.
Suite #2
San Francisco,  CA  94114
Correspondent Contact DENNIS REAGER
Regulation Number868.1400
Classification Product Code
CCK  
Date Received10/27/1992
Decision Date 04/19/1993
Decision Substantially Equivalent - Kit (SESK)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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