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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Flame Emission Photometer For Clinical Use
510(k) Number K873603
Device Name FINNIGAN MAT INCOS 50
Applicant
Finnigan Corp.
355 River Oaks Pkwy.
San Jose,  CA  95134
Applicant Contact RICHARD L MAYEUR
Correspondent
Finnigan Corp.
355 River Oaks Pkwy.
San Jose,  CA  95134
Correspondent Contact RICHARD L MAYEUR
Regulation Number862.2540
Classification Product Code
JJO  
Date Received09/04/1987
Decision Date 09/22/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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