510(k) K932685

PARAMAX(R) THEOPHYLLINE REAGENT AND CALIBRATORS by Baxter Diagnostics, Inc. — Product Code KLS

K932685 is an FDA 510(k) premarket notification submitted by Baxter Diagnostics, Inc. for the device "PARAMAX(R) THEOPHYLLINE REAGENT AND CALIBRATORS". The FDA issued a decision of Substantially Equivalent on September 24, 1993. The device falls under product code KLS (Enzyme Immunoassay, Theophylline), a Class II device regulated under 21 CFR 862.3880. Baxter Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 24, 1993
Date Received
June 3, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Theophylline
Device Class
Class II
Regulation Number
862.3880
Review Panel
TX
Submission Type