510(k) K091024

CHROMID MRSA AGAR, MODEL: REF 43 841 by bioMerieux, Inc. — Product Code JSO

K091024 is an FDA 510(k) premarket notification submitted by bioMerieux, Inc. for the device "CHROMID MRSA AGAR, MODEL: REF 43 841". The FDA issued a decision of Substantially Equivalent on July 17, 2009. The device falls under product code JSO (Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar), a Class II device regulated under 21 CFR 866.1700. bioMerieux, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 17, 2009
Date Received
April 10, 2009
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar
Device Class
Class II
Regulation Number
866.1700
Review Panel
MI
Submission Type