510(k) K874262

LAD MODEL 735 LUMINOMETER by Los Alamos Diagnostics — Product Code JJQ

K874262 is an FDA 510(k) premarket notification submitted by Los Alamos Diagnostics for the device "LAD MODEL 735 LUMINOMETER". The FDA issued a decision of Substantially Equivalent on November 27, 1987. The device falls under product code JJQ (Colorimeter, Photometer, Spectrophotometer For Clinical Use), a Class I device regulated under 21 CFR 862.2300. Los Alamos Diagnostics has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 27, 1987
Date Received
October 20, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Colorimeter, Photometer, Spectrophotometer For Clinical Use
Device Class
Class I
Regulation Number
862.2300
Review Panel
CH
Submission Type