PeriView FLEX
K-Number: K171232 · 2017-09-21
Decision Date2017-09-21
Product CodeKTI
Advisory CommitteeEN
DecisionSubstantially Equivalent
Device Summary
PeriView FLEX is a medical device manufactured by Olympus Surgical Technologies America. It received FDA 510(k) clearance on 2017-09-21 under approval number K171232. The device is classified under product code KTI. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the PeriView FLEX?
PeriView FLEX is a medical device that received FDA 510(k) clearance on 2017-09-21. It is manufactured by Olympus Surgical Technologies America. The 510(k) number is K171232.
When was PeriView FLEX approved by the FDA?
PeriView FLEX received FDA 510(k) clearance on 2017-09-21, under approval number K171232.
What company makes PeriView FLEX?
PeriView FLEX is manufactured by Olympus Surgical Technologies America.
What is the FDA product code for PeriView FLEX?
The FDA product code for PeriView FLEX is KTI.
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K193517ViziShot 2 FLEX
K212643POWERSEAL Curved Jaw Sealer and Divider, Double Action
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K163469ViziShot 2 FLEXOlympus Surgical Technologies America
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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.