510(k) K952309

N LATEX IGA by Behring Diagnostics, Inc. — Product Code CZP

K952309 is an FDA 510(k) premarket notification submitted by Behring Diagnostics, Inc. for the device "N LATEX IGA". The FDA issued a decision of Substantially Equivalent on June 20, 1995. The device falls under product code CZP (Iga, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5510. Behring Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 20, 1995
Date Received
May 17, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Iga, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5510
Review Panel
IM
Submission Type