510(k) K941317

DRIED GRAM NEGATIVE/CEFMETAZOLE by Baxter Diagnostics, Inc. — Product Code JWY

K941317 is an FDA 510(k) premarket notification submitted by Baxter Diagnostics, Inc. for the device "DRIED GRAM NEGATIVE/CEFMETAZOLE". The FDA issued a decision of Substantially Equivalent on January 31, 1995. The device falls under product code JWY (Manual Antimicrobial Susceptibility Test Systems), a Class II device regulated under 21 CFR 866.1640. Baxter Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 31, 1995
Date Received
March 18, 1994
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