510(k) K983890

SYSTEM U3 by Ab Biodisk — Product Code JWY

K983890 is an FDA 510(k) premarket notification submitted by Ab Biodisk for the device "SYSTEM U3". The FDA issued a decision of Substantially Equivalent on February 18, 1999. The device falls under product code JWY (Manual Antimicrobial Susceptibility Test Systems), a Class II device regulated under 21 CFR 866.1640. Ab Biodisk has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 18, 1999
Date Received
November 2, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Manual Antimicrobial Susceptibility Test Systems
Device Class
Class II
Regulation Number
866.1640
Review Panel
MI
Submission Type