510(k) K112276

VIZION by Trek Diagnostic Systems — Product Code JWY

K112276 is an FDA 510(k) premarket notification submitted by Trek Diagnostic Systems for the device "VIZION". The FDA issued a decision of Substantially Equivalent on November 16, 2011. The device falls under product code JWY (Manual Antimicrobial Susceptibility Test Systems), a Class II device regulated under 21 CFR 866.1640. Trek Diagnostic Systems has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 16, 2011
Date Received
August 9, 2011
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Manual Antimicrobial Susceptibility Test Systems
Device Class
Class II
Regulation Number
866.1640
Review Panel
MI
Submission Type