Contact Lens Case
K-Number: K171539 · 2017-07-14
Decision Date2017-07-14
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
Contact Lens Case is a medical device manufactured by E-Link Plastic & Metal Industrial Co.,Ltd. It received FDA 510(k) clearance on 2017-07-14 under approval number K171539. 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?
Contact Lens Case is a medical device that received FDA 510(k) clearance on 2017-07-14. It is manufactured by E-Link Plastic & Metal Industrial Co.,Ltd. The 510(k) number is K171539.
When was Contact Lens Case approved by the FDA?
Contact Lens Case received FDA 510(k) clearance on 2017-07-14, under approval number K171539.
What company makes Contact Lens Case?
Contact Lens Case is manufactured by E-Link Plastic & Metal Industrial Co.,Ltd.
What is the FDA product code for Contact Lens Case?
The FDA product code for Contact Lens Case 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.