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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Allergan, Inc.. It received FDA 510(k) clearance on 2019-08-08 under 510(k) 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. The listed applicant is Allergan, Inc.. The 510(k) number is K190674.

When did REFRESH RELIEVA For CONTACTS receive FDA 510(k) clearance?

REFRESH RELIEVA For CONTACTS received FDA 510(k) clearance on 2019-08-08, under 510(k) number K190674.

Who is the listed applicant for REFRESH RELIEVA For CONTACTS?

The FDA 510(k) record lists Allergan, Inc. as the applicant. This does not by itself establish the device manufacturer.

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.

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