RIGID GAS PERMEABLE CONTACT LENS SOLUTION
K-Number: K983836 · 1999-02-11
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Device Summary
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.
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