Sporview VH202 BI
K-Number: K171287 · 2018-02-01
Decision Date2018-02-01
Product CodeFRC
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Sporview VH202 BI is a medical device manufactured by Spsmedical Supply Corp. A Division of Cantel Medical. It received FDA 510(k) clearance on 2018-02-01 under approval number K171287. The device is classified under product code FRC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Sporview VH202 BI?
Sporview VH202 BI is a medical device that received FDA 510(k) clearance on 2018-02-01. It is manufactured by Spsmedical Supply Corp. A Division of Cantel Medical. The 510(k) number is K171287.
When was Sporview VH202 BI approved by the FDA?
Sporview VH202 BI received FDA 510(k) clearance on 2018-02-01, under approval number K171287.
What company makes Sporview VH202 BI?
Sporview VH202 BI is manufactured by Spsmedical Supply Corp. A Division of Cantel Medical.
What is the FDA product code for Sporview VH202 BI?
The FDA product code for Sporview VH202 BI is FRC.
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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.