510(k) K113177

COMPLETE D 25-OH VITAMIN D CONTROL by Quantimetrix Corp. — Product Code JJX

K113177 is an FDA 510(k) premarket notification submitted by Quantimetrix Corp. for the device "COMPLETE D 25-OH VITAMIN D CONTROL". The FDA issued a decision of Substantially Equivalent on May 10, 2012. The device falls under product code JJX (Single (Specified) Analyte Controls (Assayed And Unassayed)), a Class I device regulated under 21 CFR 862.1660. Quantimetrix Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 10, 2012
Date Received
October 28, 2011
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Single (Specified) Analyte Controls (Assayed And Unassayed)
Device Class
Class I
Regulation Number
862.1660
Review Panel
CH
Submission Type