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FDA 510(k)

OPTI-ONE MULTI-PURPOSE SOLUTION

K-Number: K983973 · 1998-12-18

ApplicantAlcon Laboratories
Decision Date1998-12-18
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPTI-ONE MULTI-PURPOSE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories. It received FDA 510(k) clearance on 1998-12-18 under 510(k) number K983973. The device is classified under product code LPN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTI-ONE MULTI-PURPOSE SOLUTION?

OPTI-ONE MULTI-PURPOSE SOLUTION is a medical device that received FDA 510(k) clearance on 1998-12-18. The listed applicant is Alcon Laboratories. The 510(k) number is K983973.

When did OPTI-ONE MULTI-PURPOSE SOLUTION receive FDA 510(k) clearance?

OPTI-ONE MULTI-PURPOSE SOLUTION received FDA 510(k) clearance on 1998-12-18, under 510(k) number K983973.

Who is the listed applicant for OPTI-ONE MULTI-PURPOSE SOLUTION?

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 OPTI-ONE MULTI-PURPOSE SOLUTION?

The FDA product code for OPTI-ONE MULTI-PURPOSE SOLUTION is LPN.

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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.

K062624NEXT GENERATION LASERK062865SMALL VOLUME SYRINGEK000148RGP MULTI-PURPOSE SOLUTION ID 100136K984573OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROPK990480OPTI-FREE SUPRACLENS DAILY PROTEIN REMOVERK984575MULTI-PURPOSE DISINFECTING SOLUTION ID 90746

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Related Devices (Code: LPN)

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.

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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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