Contact Lens Case Round Glasses
K-Number: K171163 · 2017-06-27
ApplicantFiftytwoways, Ltd.
Decision Date2017-06-27
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
Contact Lens Case Round Glasses is a medical device manufactured by Fiftytwoways, Ltd.. It received FDA 510(k) clearance on 2017-06-27 under approval number K171163. The device is classified under product code LRX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Contact Lens Case Round Glasses?
Contact Lens Case Round Glasses is a medical device that received FDA 510(k) clearance on 2017-06-27. It is manufactured by Fiftytwoways, Ltd.. The 510(k) number is K171163.
When was Contact Lens Case Round Glasses approved by the FDA?
Contact Lens Case Round Glasses received FDA 510(k) clearance on 2017-06-27, under approval number K171163.
What company makes Contact Lens Case Round Glasses?
Contact Lens Case Round Glasses is manufactured by Fiftytwoways, Ltd..
What is the FDA product code for Contact Lens Case Round Glasses?
The FDA product code for Contact Lens Case Round Glasses is LRX.
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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.