FDA 510(k)

K-SOL

K-Number: K844249 · 1985-04-30

Decision Date1985-04-30

Product CodeLYX

DecisionSubstantially Equivalent

Device Summary

K-SOL is the device name listed in this FDA 510(k) record. The listed applicant is Cilco, Inc.. It received FDA 510(k) clearance on 1985-04-30 under 510(k) number K844249. The device is classified under product code LYX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the K-SOL?

K-SOL is a medical device that received FDA 510(k) clearance on 1985-04-30. The listed applicant is Cilco, Inc.. The 510(k) number is K844249.

When did K-SOL receive FDA 510(k) clearance?

K-SOL received FDA 510(k) clearance on 1985-04-30, under 510(k) number K844249.

Who is the listed applicant for K-SOL?

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

What is the FDA product code for K-SOL?

The FDA product code for K-SOL is LYX.

Other records listing Cilco, Inc. 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.

K861334CILCO DIAMOND KNIVES & DIAMOND KNIFE LINEAR GAUGE K854969CILCO SONOMETRICS A&B DIGITAL SYSTEM (DIGISCAN)K843319CILCO I/A SURGICAL PACK K843992CILCOR OPHTHALMIC INSTRUMENTS K843447CILCO DIAMOND KNIFE K841099OCTOPUS 500/500E

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Related Devices (Code: LYX)

K251320XTRA4Al.Chi.Mi.A. S.R.L K221759CornisolAurolab K211786Independent Corneal Viewing Chamber (IVC-21)Bausch + Lomb, Incorporated K162013Eusol-CAl.Chi.Mi.A. S.R.L K063304LIFE4CNumedis, Inc.K063617EUSOL-CAl.Chi.Mi.A

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.