ALL-IN-ONE HARD CONTACT LENS SOLUTION
K-Number: K853807 · 1985-12-16
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Device Summary
Frequently Asked Questions
What is the ALL-IN-ONE HARD CONTACT LENS SOLUTION?
ALL-IN-ONE HARD CONTACT LENS SOLUTION is a medical device that received FDA 510(k) clearance on 1985-12-16. The listed applicant is Maurry Biological Co.. The 510(k) number is K853807.
When did ALL-IN-ONE HARD CONTACT LENS SOLUTION receive FDA 510(k) clearance?
ALL-IN-ONE HARD CONTACT LENS SOLUTION received FDA 510(k) clearance on 1985-12-16, under 510(k) number K853807.
Who is the listed applicant for ALL-IN-ONE HARD CONTACT LENS SOLUTION?
The FDA 510(k) record lists Maurry Biological Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALL-IN-ONE HARD CONTACT LENS SOLUTION?
The FDA product code for ALL-IN-ONE HARD CONTACT LENS SOLUTION is HPX.
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 Maurry Biological Co. 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: HPX)
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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