510(k) K850995

SMART ALEX COMPACT CLINICAL ANALYZER(CCA)(FILTER P by Awareness Technology, Inc. — Product Code JJQ

K850995 is an FDA 510(k) premarket notification submitted by Awareness Technology, Inc. for the device "SMART ALEX COMPACT CLINICAL ANALYZER(CCA)(FILTER P". The FDA issued a decision of Substantially Equivalent on May 10, 1985. The device falls under product code JJQ (Colorimeter, Photometer, Spectrophotometer For Clinical Use), a Class I device regulated under 21 CFR 862.2300. Awareness Technology, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 10, 1985
Date Received
March 11, 1985
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