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FDA 510(k)

LENSKEEPER CONTACT LENS CARRYING CASE

K-Number: K861642 · 1986-05-29

Decision Date1986-05-29
Product CodeHPX
DecisionSubstantially Equivalent

Device Summary

LENSKEEPER CONTACT LENS CARRYING CASE is the device name listed in this FDA 510(k) record. The listed applicant is Allergan, Inc.. It received FDA 510(k) clearance on 1986-05-29 under 510(k) number K861642. The device is classified under product code HPX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LENSKEEPER CONTACT LENS CARRYING CASE?

LENSKEEPER CONTACT LENS CARRYING CASE is a medical device that received FDA 510(k) clearance on 1986-05-29. The listed applicant is Allergan, Inc.. The 510(k) number is K861642.

When did LENSKEEPER CONTACT LENS CARRYING CASE receive FDA 510(k) clearance?

LENSKEEPER CONTACT LENS CARRYING CASE received FDA 510(k) clearance on 1986-05-29, under 510(k) number K861642.

Who is the listed applicant for LENSKEEPER CONTACT LENS CARRYING CASE?

The FDA 510(k) record lists Allergan, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LENSKEEPER CONTACT LENS CARRYING CASE?

The FDA product code for LENSKEEPER CONTACT LENS CARRYING CASE 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 Allergan, 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.

View all 32 devices →

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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