Contact Lens Case Round Glasses
K-Number: K171163 · 2017-06-27
Device Summary
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. The listed applicant is Fiftytwoways, Ltd.. The 510(k) number is K171163.
When did Contact Lens Case Round Glasses receive FDA 510(k) clearance?
Contact Lens Case Round Glasses received FDA 510(k) clearance on 2017-06-27, under 510(k) number K171163.
Who is the listed applicant for Contact Lens Case Round Glasses?
The FDA 510(k) record lists Fiftytwoways, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Contact Lens Case Round Glasses?
The FDA product code for Contact Lens Case Round Glasses is LRX.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LRX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.