Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K833292Substantially Equivalent

Lactabacillus Agar W/o Tween80

Neogen Culture Media, Mchenry IL / Traditional, Substantially Equivalent

K833292 is the FDA 510(k) clearance record for LACTABACILLUS AGAR W/O TWEEN80, cleared for Acumedia Manufacturers, Inc. on . FDA records list 177 510(k) clearances for Neogen Culture Media, from to . As of , FDA records show no recalls naming K833292.

Clearance record

Decision date
Received
(53 days to decision)
Review panel
Unknown
Applicant
Acumedia Manufacturers, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No