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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Kit, Quality Control For Culture Media
510(k) Number K830133
Device Name Q-CHECK CULTI-LOOPS
Applicant
Lab Ability, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Lab Ability, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number866.2480
Classification Product Code
JTR  
Date Received01/13/1983
Decision Date 02/09/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Immunology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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