ALLERGAN LENS CASE
K-Number: K884251 · 1988-12-28
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Device Summary
Frequently Asked Questions
What is the ALLERGAN LENS CASE?
ALLERGAN LENS CASE is a medical device that received FDA 510(k) clearance on 1988-12-28. The listed applicant is Allergan Optical. The 510(k) number is K884251.
When did ALLERGAN LENS CASE receive FDA 510(k) clearance?
ALLERGAN LENS CASE received FDA 510(k) clearance on 1988-12-28, under 510(k) number K884251.
Who is the listed applicant for ALLERGAN LENS CASE?
The FDA 510(k) record lists Allergan Optical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALLERGAN LENS CASE?
The FDA product code for ALLERGAN LENS CASE 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.
Other records listing Allergan Optical as applicant
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.
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