510(k) K960313

MUELLER HINTON AGAR WITH 2% NACI by Remel, L.P. — Product Code JTZ

K960313 is an FDA 510(k) premarket notification submitted by Remel, L.P. for the device "MUELLER HINTON AGAR WITH 2% NACI". The FDA issued a decision of Substantially Equivalent on March 25, 1996. 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. Remel, L.P. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 25, 1996
Date Received
January 22, 1996
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