510(k) K822119

ACCESSORY MEDIA FOR FLOW TITERTEK MIC by Flow Laboratories, Inc. — Product Code JTZ

K822119 is an FDA 510(k) premarket notification submitted by Flow Laboratories, Inc. for the device "ACCESSORY MEDIA FOR FLOW TITERTEK MIC". The FDA issued a decision of Substantially Equivalent on August 3, 1982. The device falls under product code JTZ (Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth), a Class II device regulated under 21 CFR 866.1700. Flow Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 3, 1982
Date Received
July 19, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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