510(k) K854875

APO-SCREEN CALIBRATOR & CONTROL SET FOR HDL APO A1 by Photec Diagnostics, Inc. — Product Code DER

K854875 is an FDA 510(k) premarket notification submitted by Photec Diagnostics, Inc. for the device "APO-SCREEN CALIBRATOR & CONTROL SET FOR HDL APO A1". The FDA issued a decision of Substantially Equivalent on January 24, 1986. The device falls under product code DER (Alpha-1-Lipoprotein, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5580. Photec Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 24, 1986
Date Received
December 4, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Alpha-1-Lipoprotein, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5580
Review Panel
IM
Submission Type