K-SOL(TM)
K-Number: K911587 · 1991-11-01
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Device Summary
Frequently Asked Questions
What is the K-SOL(TM)?
K-SOL(TM) is a medical device that received FDA 510(k) clearance on 1991-11-01. The listed applicant is Alcon Laboratories. The 510(k) number is K911587.
When did K-SOL(TM) receive FDA 510(k) clearance?
K-SOL(TM) received FDA 510(k) clearance on 1991-11-01, under 510(k) number K911587.
Who is the listed applicant for K-SOL(TM)?
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 K-SOL(TM)?
The FDA product code for K-SOL(TM) is KDN.
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: KDN)
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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