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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Aggregometer, Platelet, Photo-Optical Scanning
510(k) Number K771198
Device Name LUMI-AGGREGOMETER
Applicant
Chrono-Log Corp.
2 W. Park Rd.
Havertown,  PA  19083
Applicant Contact Arthur Freilich
Correspondent
Chrono-Log Corp.
2 W. Park Rd.
Havertown,  PA  19083
Correspondent Contact Arthur Freilich
Regulation Number864.6675
Classification Product Code
JBY  
Date Received07/01/1977
Decision Date 08/02/1977
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Hematology
510k Review Panel Hematology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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