TSE-ANDERSON MODIFIED LACRIMAL GROOV
K-Number: K840861 · 1984-05-09
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Device Summary
Frequently Asked Questions
What is the TSE-ANDERSON MODIFIED LACRIMAL GROOV?
TSE-ANDERSON MODIFIED LACRIMAL GROOV is a medical device that received FDA 510(k) clearance on 1984-05-09. The listed applicant is Hansen Ophthalmic Development Lab. The 510(k) number is K840861.
When did TSE-ANDERSON MODIFIED LACRIMAL GROOV receive FDA 510(k) clearance?
TSE-ANDERSON MODIFIED LACRIMAL GROOV received FDA 510(k) clearance on 1984-05-09, under 510(k) number K840861.
Who is the listed applicant for TSE-ANDERSON MODIFIED LACRIMAL GROOV?
The FDA 510(k) record lists Hansen Ophthalmic Development Lab as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TSE-ANDERSON MODIFIED LACRIMAL GROOV?
The FDA product code for TSE-ANDERSON MODIFIED LACRIMAL GROOV is HNL.
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.
Related Devices (Code: HNL)
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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