510(k) K850832

CAMPYLOBACTER BLOOD-FREE SELECTIVE AGAR BASEQ by Oxoid U.S.A., Inc. — Product Code JSJ

K850832 is an FDA 510(k) premarket notification submitted by Oxoid U.S.A., Inc. for the device "CAMPYLOBACTER BLOOD-FREE SELECTIVE AGAR BASEQ". The FDA issued a decision of Substantially Equivalent on March 29, 1985. The device falls under product code JSJ (Culture Media, Selective And Non-Differential), a Class I device regulated under 21 CFR 866.2360. Oxoid U.S.A., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 29, 1985
Date Received
February 15, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Culture Media, Selective And Non-Differential
Device Class
Class I
Regulation Number
866.2360
Review Panel
MI
Submission Type