510(k) K941030

DRIED GRAM-NEGATIVE CEFPODOXIME by Baxter Diagnostics, Inc. — Product Code LTT

K941030 is an FDA 510(k) premarket notification submitted by Baxter Diagnostics, Inc. for the device "DRIED GRAM-NEGATIVE CEFPODOXIME". The FDA issued a decision of Substantially Equivalent on February 16, 1995. The device falls under product code LTT (Panels, Test, Susceptibility, Antimicrobial), 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
February 16, 1995
Date Received
March 4, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Panels, Test, Susceptibility, Antimicrobial
Device Class
Class II
Regulation Number
866.1640
Review Panel
MI
Submission Type