ALCON CONTACT LENS CASE
K-Number: K971618 · 1997-07-14
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Device Summary
Frequently Asked Questions
What is the ALCON CONTACT LENS CASE?
ALCON CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 1997-07-14. The listed applicant is Alcon Laboratories. The 510(k) number is K971618.
When did ALCON CONTACT LENS CASE receive FDA 510(k) clearance?
ALCON CONTACT LENS CASE received FDA 510(k) clearance on 1997-07-14, under 510(k) number K971618.
Who is the listed applicant for ALCON CONTACT LENS CASE?
The FDA 510(k) record lists Alcon Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALCON CONTACT LENS CASE?
The FDA product code for ALCON CONTACT 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 Alcon Laboratories 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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