510(k) K951241

HAEMOPHILUS/PNEUMOCOCCUS MIC PLATE by Radiometer America, Inc. — Product Code JWY

K951241 is an FDA 510(k) premarket notification submitted by Radiometer America, Inc. for the device "HAEMOPHILUS/PNEUMOCOCCUS MIC PLATE". The FDA issued a decision of Substantially Equivalent on October 7, 1995. The device falls under product code JWY (Manual Antimicrobial Susceptibility Test Systems), a Class II device regulated under 21 CFR 866.1640. Radiometer America, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 7, 1995
Date Received
February 27, 1995
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