Contact Lens Case, Model: A-1, B-1
K-Number: K172925 · 2017-11-30
ApplicantP L Overseas Limited
Decision Date2017-11-30
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
Contact Lens Case, Model: A-1, B-1 is a medical device manufactured by P L Overseas Limited. It received FDA 510(k) clearance on 2017-11-30 under approval number K172925. 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, Model: A-1, B-1?
Contact Lens Case, Model: A-1, B-1 is a medical device that received FDA 510(k) clearance on 2017-11-30. It is manufactured by P L Overseas Limited. The 510(k) number is K172925.
When was Contact Lens Case, Model: A-1, B-1 approved by the FDA?
Contact Lens Case, Model: A-1, B-1 received FDA 510(k) clearance on 2017-11-30, under approval number K172925.
What company makes Contact Lens Case, Model: A-1, B-1?
Contact Lens Case, Model: A-1, B-1 is manufactured by P L Overseas Limited.
What is the FDA product code for Contact Lens Case, Model: A-1, B-1?
The FDA product code for Contact Lens Case, Model: A-1, B-1 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.