Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

RIGID GAS PERMEABLE CONTACT LENS SOLUTION

K-Number: K983836 · 1999-02-11

Decision Date1999-02-11
Product CodeMRC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RIGID GAS PERMEABLE CONTACT LENS SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Polymer Technology Div. Wilmington Partners, L.P.. It received FDA 510(k) clearance on 1999-02-11 under 510(k) number K983836. 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 RIGID GAS PERMEABLE CONTACT LENS SOLUTION?

RIGID GAS PERMEABLE CONTACT LENS SOLUTION is a medical device that received FDA 510(k) clearance on 1999-02-11. The listed applicant is Polymer Technology Div. Wilmington Partners, L.P.. The 510(k) number is K983836.

When did RIGID GAS PERMEABLE CONTACT LENS SOLUTION receive FDA 510(k) clearance?

RIGID GAS PERMEABLE CONTACT LENS SOLUTION received FDA 510(k) clearance on 1999-02-11, under 510(k) number K983836.

Who is the listed applicant for RIGID GAS PERMEABLE CONTACT LENS SOLUTION?

The FDA 510(k) record lists Polymer Technology Div. Wilmington Partners, L.P. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RIGID GAS PERMEABLE CONTACT LENS SOLUTION?

The FDA product code for RIGID GAS PERMEABLE CONTACT LENS SOLUTION is MRC.

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 Polymer Technology Div. Wilmington Partners, L.P. 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.

Related Devices (Code: MRC)

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.

↑