FDA 510(k)

SOLO-CARE BRAND MULTI-PURPOSE SOLUTION

K-Number: K983291 · 1998-11-25

Decision Date1998-11-25

Product CodeMRC

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 1998-11-25 under 510(k) number K983291. The device is classified under product code MRC. 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 1998-11-25. The listed applicant is Ciba Vision Corporation. The 510(k) number is K983291.

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 1998-11-25, under 510(k) number K983291.

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 MRC.

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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.