510(k) K170678

Beta-CrossLaps CalCheck 5 by Roche Diagnostics — Product Code JJX

K170678 is an FDA 510(k) premarket notification submitted by Roche Diagnostics for the device "Beta-CrossLaps CalCheck 5". The FDA issued a decision of Substantially Equivalent on April 4, 2017. The device falls under product code JJX (Single (Specified) Analyte Controls (Assayed And Unassayed)), a Class I device regulated under 21 CFR 862.1660. Roche Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 4, 2017
Date Received
March 6, 2017
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