510(k) K882351

MUELLER HINTON AGAR PLATES P3318/1&2/P3418/P34181 by Lakewood Biochemical Co., Inc. — Product Code JTZ

K882351 is an FDA 510(k) premarket notification submitted by Lakewood Biochemical Co., Inc. for the device "MUELLER HINTON AGAR PLATES P3318/1&2/P3418/P34181". The FDA issued a decision of Substantially Equivalent on June 28, 1988. 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. Lakewood Biochemical Co., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 28, 1988
Date Received
June 7, 1988
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