REFRESH RELIEVA For CONTACTS
K-Number: K190674 · 2019-08-08
ApplicantAllergan, Inc.
Decision Date2019-08-08
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
REFRESH RELIEVA For CONTACTS is a medical device manufactured by Allergan, Inc.. It received FDA 510(k) clearance on 2019-08-08 under approval number K190674. The device is classified under product code LPN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the REFRESH RELIEVA For CONTACTS?
REFRESH RELIEVA For CONTACTS is a medical device that received FDA 510(k) clearance on 2019-08-08. It is manufactured by Allergan, Inc.. The 510(k) number is K190674.
When was REFRESH RELIEVA For CONTACTS approved by the FDA?
REFRESH RELIEVA For CONTACTS received FDA 510(k) clearance on 2019-08-08, under approval number K190674.
What company makes REFRESH RELIEVA For CONTACTS?
REFRESH RELIEVA For CONTACTS is manufactured by Allergan, Inc..
What is the FDA product code for REFRESH RELIEVA For CONTACTS?
The FDA product code for REFRESH RELIEVA For CONTACTS is LPN.
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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.