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FDA 510(k) Application Details - K193340
Device Classification Name
System, Test, Blood Glucose, Over The Counter
More FDA Info for this Device
510(K) Number
K193340
Device Name
System, Test, Blood Glucose, Over The Counter
Applicant
MicroTech Medical, Inc.
3350 Scott Blvd, Bldg.64
Santa Clara, CA 95045 US
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Contact
Dore Mark
Other 510(k) Applications for this Contact
Regulation Number
862.1345
More FDA Info for this Regulation Number
Classification Product Code
NBW
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/02/2019
Decision Date
09/11/2020
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CH - Clinical Chemistry
Review Advisory Committee
CH - Clinical Chemistry
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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