510(k) K112742

AUDIT MICROLQ SPINAL FLUID CONTROL by Aalto Scientific, Ltd. — Product Code JJY

K112742 is an FDA 510(k) premarket notification submitted by Aalto Scientific, Ltd. for the device "AUDIT MICROLQ SPINAL FLUID CONTROL". The FDA issued a decision of Substantially Equivalent on June 15, 2012. The device falls under product code JJY (Multi-Analyte Controls, All Kinds (Assayed)), a Class I device regulated under 21 CFR 862.1660. Aalto Scientific, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 15, 2012
Date Received
September 21, 2011
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Multi-Analyte Controls, All Kinds (Assayed)
Device Class
Class I
Regulation Number
862.1660
Review Panel
CH
Submission Type