Vista Solution Monitoring Kit, Vista Solution 2 10-day Evaluation Kit, VistaTablet 2 (Boxed)
K-Number: K193343 · 2020-04-20
ApplicantVitalconnect, Inc.
Decision Date2020-04-20
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Vista Solution Monitoring Kit, Vista Solution 2 10-day Evaluation Kit, VistaTablet 2 (Boxed) is a medical device manufactured by Vitalconnect, Inc.. It received FDA 510(k) clearance on 2020-04-20 under approval number K193343. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Vista Solution Monitoring Kit, Vista Solution 2 10-day Evaluation Kit, VistaTablet 2 (Boxed)?
Vista Solution Monitoring Kit, Vista Solution 2 10-day Evaluation Kit, VistaTablet 2 (Boxed) is a medical device that received FDA 510(k) clearance on 2020-04-20. It is manufactured by Vitalconnect, Inc.. The 510(k) number is K193343.
When was Vista Solution Monitoring Kit, Vista Solution 2 10-day Evaluation Kit, VistaTablet 2 (Boxed) approved by the FDA?
Vista Solution Monitoring Kit, Vista Solution 2 10-day Evaluation Kit, VistaTablet 2 (Boxed) received FDA 510(k) clearance on 2020-04-20, under approval number K193343.
What company makes Vista Solution Monitoring Kit, Vista Solution 2 10-day Evaluation Kit, VistaTablet 2 (Boxed)?
Vista Solution Monitoring Kit, Vista Solution 2 10-day Evaluation Kit, VistaTablet 2 (Boxed) is manufactured by Vitalconnect, Inc..
What is the FDA product code for Vista Solution Monitoring Kit, Vista Solution 2 10-day Evaluation Kit, VistaTablet 2 (Boxed)?
The FDA product code for Vista Solution Monitoring Kit, Vista Solution 2 10-day Evaluation Kit, VistaTablet 2 (Boxed) is DRG.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.