HERRICK LACRIMAL PLUG TM.
K-Number: K896175 · 1990-01-22
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Device Summary
Frequently Asked Questions
What is the HERRICK LACRIMAL PLUG TM.?
HERRICK LACRIMAL PLUG TM. is a medical device that received FDA 510(k) clearance on 1990-01-22. The listed applicant is Lacrimedics, Inc.. The 510(k) number is K896175.
When did HERRICK LACRIMAL PLUG TM. receive FDA 510(k) clearance?
HERRICK LACRIMAL PLUG TM. received FDA 510(k) clearance on 1990-01-22, under 510(k) number K896175.
Who is the listed applicant for HERRICK LACRIMAL PLUG 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 HERRICK LACRIMAL PLUG TM.?
The FDA product code for HERRICK LACRIMAL PLUG 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.
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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