VISALENS ALL PURPOSE SOLUTION FOR LENS
K-Number: K791523 · 1980-02-19
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Device Summary
Frequently Asked Questions
What is the VISALENS ALL PURPOSE SOLUTION FOR LENS?
VISALENS ALL PURPOSE SOLUTION FOR LENS is a medical device that received FDA 510(k) clearance on 1980-02-19. The listed applicant is Pfizer, Inc.. The 510(k) number is K791523.
When did VISALENS ALL PURPOSE SOLUTION FOR LENS receive FDA 510(k) clearance?
VISALENS ALL PURPOSE SOLUTION FOR LENS received FDA 510(k) clearance on 1980-02-19, under 510(k) number K791523.
Who is the listed applicant for VISALENS ALL PURPOSE SOLUTION FOR LENS?
The FDA 510(k) record lists Pfizer, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VISALENS ALL PURPOSE SOLUTION FOR LENS?
The FDA product code for VISALENS ALL PURPOSE SOLUTION FOR LENS 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 Pfizer, Inc. 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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