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FDA 510(k)

SOLO-CARE BRAND MULTI-PURPOSE SOLUTION

K-Number: K982168 · 1998-11-17

Decision Date1998-11-17
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SOLO-CARE BRAND MULTI-PURPOSE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Ciba Vision Corporation. It received FDA 510(k) clearance on 1998-11-17 under 510(k) number K982168. 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 SOLO-CARE BRAND MULTI-PURPOSE SOLUTION?

SOLO-CARE BRAND MULTI-PURPOSE SOLUTION is a medical device that received FDA 510(k) clearance on 1998-11-17. The listed applicant is Ciba Vision Corporation. The 510(k) number is K982168.

When did SOLO-CARE BRAND MULTI-PURPOSE SOLUTION receive FDA 510(k) clearance?

SOLO-CARE BRAND MULTI-PURPOSE SOLUTION received FDA 510(k) clearance on 1998-11-17, under 510(k) number K982168.

Who is the listed applicant for SOLO-CARE BRAND MULTI-PURPOSE SOLUTION?

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

What is the FDA product code for SOLO-CARE BRAND MULTI-PURPOSE SOLUTION?

The FDA product code for SOLO-CARE BRAND MULTI-PURPOSE SOLUTION is LPN.

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 Ciba Vision Corporation 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 43 devices →

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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