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FDA 510(k)

VISALENS ALL PURPOSE SOLUTION FOR LENS

K-Number: K791523 · 1980-02-19

ApplicantPfizer, Inc.
Decision Date1980-02-19
Product CodeHPX
DecisionSubstantially Equivalent

Device Summary

VISALENS ALL PURPOSE SOLUTION FOR LENS is the device name listed in this FDA 510(k) record. The listed applicant is Pfizer, Inc.. It received FDA 510(k) clearance on 1980-02-19 under 510(k) number K791523. The device is classified under product code HPX. FDA Decision: Substantially Equivalent.

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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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