Vizion

FDA 510(k) K112276 · Trek Diagnostic Systems

Substantially Equivalent

510(k) numberK112276

Submission

Device name
Vizion
Applicant
Trek Diagnostic Systems
Cleveland, OH, US
Received
August 9, 2011
Decision date
November 16, 2011
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JWY – Manual Antimicrobial Susceptibility Test Systems
Device class
Class II (moderate risk)
Regulation
21 CFR 866.1640
Specialty
Microbiology

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K250990The Sensititre 18-24 hour MIC or Breakpoint Susceptibility System with Ciprofloxacin in…JWY · Traditional Thermo Fisher Scientific06/30/2025SE
K242843The Sensititre 20-24 hour Haemophilus influenzae/Streptococcus pneumoniae (HP) MIC or…JWY · Traditional Thermo Fisher Scientific06/20/2025SE
K250856ETEST Aztreonam/Avibactam (AZA) (0.016/4-256/4 µg/mL)JWY · Traditional Biomérieux06/12/2025SE

More from Biomérieux

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K103532Autoreader 2LRG · Traditional 08/26/2011SE
K111429Sensititre (R) HP Mic Susceptibility Plate with Cefaroline (0.004-8UG/ML) and the…JWY · Traditional 08/18/2011SE
K103456The Sensititre AimLIE · Traditional 06/22/2011SE
K110331Sensititre Aim (TM)LIE · Traditional 04/27/2011SE
K093741Sensitive Haemophilus Influenzae, Streptococcus Pneumonia, (HP) Mic Susceptibility PlatesJWY · Traditional 02/25/2010SE
K093865Sensititre 18-24HR Susceptibility PlatesJWY · Traditional 02/17/2010SE
K092445Sensititre 18-24 Hour Susceptibility PlatesJWY · Traditional 12/16/2009SE

Questions and answers

When was Vizion cleared by the FDA?

Vizion (K112276) received a 510(k) decision of Substantially Equivalent on November 16, 2011, 99 days after the submission was received.

What is the product code of K112276?

The FDA product code is JWY – Manual Antimicrobial Susceptibility Test Systems, a Class II (moderate risk) device regulated under 21 CFR 866.1640.