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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name device, microtiter diluting/dispensing
510(k) Number K871945
Device Name MICROLAB AT
Applicant
HAMILTON CO.
POST OFFICE BOX 10030
RENO,  NV  89520
Applicant Contact KEN LINDNER
Correspondent
HAMILTON CO.
POST OFFICE BOX 10030
RENO,  NV  89520
Correspondent Contact KEN LINDNER
Regulation Number866.2500
Classification Product Code
JTC  
Date Received05/19/1987
Decision Date 05/29/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Microbiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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