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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Spinner, Slide, Automated
510(k) Number K771898
Device Name AUTOMATED SLIDE SPINNER
Applicant
Dynatech Cryomedical Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Dynatech Cryomedical Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number864.5850
Classification Product Code
GKJ  
Date Received10/06/1977
Decision Date 10/18/1977
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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