510(k) K881533

BLOOD AGAR BASE NO. 2 by Acumedia Manufacturers, Inc. — Product Code JSG

K881533 is an FDA 510(k) premarket notification submitted by Acumedia Manufacturers, Inc. for the device "BLOOD AGAR BASE NO. 2". The FDA issued a decision of Substantially Equivalent on April 18, 1988. The device falls under product code JSG (Culture Media, Non-Selective And Non-Differential), a Class I device regulated under 21 CFR 866.2300. Acumedia Manufacturers, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 18, 1988
Date Received
April 8, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Culture Media, Non-Selective And Non-Differential
Device Class
Class I
Regulation Number
866.2300
Review Panel
MI
Submission Type