510(k) K964527

N RHEUMATOLOGY STANDARD SL by Behring Diagnostics, Inc. — Product Code JIX

K964527 is an FDA 510(k) premarket notification submitted by Behring Diagnostics, Inc. for the device "N RHEUMATOLOGY STANDARD SL". The FDA issued a decision of Substantially Equivalent on January 15, 1997. The device falls under product code JIX (Calibrator, Multi-Analyte Mixture), a Class II device regulated under 21 CFR 862.1150. Behring Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 15, 1997
Date Received
November 12, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Calibrator, Multi-Analyte Mixture
Device Class
Class II
Regulation Number
862.1150
Review Panel
CH
Submission Type