Contact Lens Case
K-Number: K162869 · 2016-12-09
Decision Date2016-12-09
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
Contact Lens Case is a medical device manufactured by Ningbo Yinzhou Zonghai Artware Co., Ltd.. It received FDA 510(k) clearance on 2016-12-09 under approval number K162869. 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 2016-12-09. It is manufactured by Ningbo Yinzhou Zonghai Artware Co., Ltd.. The 510(k) number is K162869.
When was Contact Lens Case approved by the FDA?
Contact Lens Case received FDA 510(k) clearance on 2016-12-09, under approval number K162869.
What company makes Contact Lens Case?
Contact Lens Case is manufactured by Ningbo Yinzhou Zonghai Artware 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.