510(k) K851912

LASER PREALBUMIN TEST by Behring Diagnostics, Inc. — Product Code JZJ

K851912 is an FDA 510(k) premarket notification submitted by Behring Diagnostics, Inc. for the device "LASER PREALBUMIN TEST". The FDA issued a decision of Substantially Equivalent on June 21, 1985. The device falls under product code JZJ (Prealbumin, Antigen, Antiserum, Control), a Class I device regulated under 21 CFR 866.5060. Behring Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 21, 1985
Date Received
May 1, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prealbumin, Antigen, Antiserum, Control
Device Class
Class I
Regulation Number
866.5060
Review Panel
IM
Submission Type