510(k) K936305

SENSITITRE/PIP/TA2 SUSCEPTIBILITY PLATES by Radiometer America, Inc. — Product Code JWY

K936305 is an FDA 510(k) premarket notification submitted by Radiometer America, Inc. for the device "SENSITITRE/PIP/TA2 SUSCEPTIBILITY PLATES". The FDA issued a decision of Substantially Equivalent on July 13, 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
July 13, 1995
Date Received
December 21, 1993
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