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FDA 510(k)

OPTISOL

K-Number: K894162 · 1990-01-12

Decision Date1990-01-12
Product CodeLYX
DecisionSubstantially Equivalent

Device Summary

OPTISOL is the device name listed in this FDA 510(k) record. The listed applicant is Chiron Ophthalmics. It received FDA 510(k) clearance on 1990-01-12 under 510(k) number K894162. The device is classified under product code LYX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTISOL?

OPTISOL is a medical device that received FDA 510(k) clearance on 1990-01-12. The listed applicant is Chiron Ophthalmics. The 510(k) number is K894162.

When did OPTISOL receive FDA 510(k) clearance?

OPTISOL received FDA 510(k) clearance on 1990-01-12, under 510(k) number K894162.

Who is the listed applicant for OPTISOL?

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

What is the FDA product code for OPTISOL?

The FDA product code for OPTISOL is LYX.

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 Chiron Ophthalmics 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.

View all 10 devices →

Related Devices (Code: LYX)

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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