510(k) K091914

OMNIS HEALTH EMBRACE GLUCOSE CONTROL SOLUTION by Bionostics, Inc. — Product Code JJX

K091914 is an FDA 510(k) premarket notification submitted by Bionostics, Inc. for the device "OMNIS HEALTH EMBRACE GLUCOSE CONTROL SOLUTION". The FDA issued a decision of Substantially Equivalent on November 6, 2009. The device falls under product code JJX (Single (Specified) Analyte Controls (Assayed And Unassayed)), a Class I device regulated under 21 CFR 862.1660. Bionostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 6, 2009
Date Received
June 30, 2009
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