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FDA 510(k)

LACRIMAL EFFICIENCY TEST (TM)

K-Number: K890714 · 1989-05-17

Decision Date1989-05-17
Product CodeLZU
DecisionSubstantially Equivalent

Device Summary

LACRIMAL EFFICIENCY TEST (TM) is the device name listed in this FDA 510(k) record. The listed applicant is Lacrimedics, Inc.. It received FDA 510(k) clearance on 1989-05-17 under 510(k) number K890714. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LACRIMAL EFFICIENCY TEST (TM)?

LACRIMAL EFFICIENCY TEST (TM) is a medical device that received FDA 510(k) clearance on 1989-05-17. The listed applicant is Lacrimedics, Inc.. The 510(k) number is K890714.

When did LACRIMAL EFFICIENCY TEST (TM) receive FDA 510(k) clearance?

LACRIMAL EFFICIENCY TEST (TM) received FDA 510(k) clearance on 1989-05-17, under 510(k) number K890714.

Who is the listed applicant for LACRIMAL EFFICIENCY TEST (TM)?

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

What is the FDA product code for LACRIMAL EFFICIENCY TEST (TM)?

The FDA product code for LACRIMAL EFFICIENCY TEST (TM) is LZU.

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 Lacrimedics, 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 11 devices →

Related Devices (Code: LZU)

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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