Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TSE-ANDERSON MODIFIED LACRIMAL GROOV

K-Number: K840861 · 1984-05-09

Decision Date1984-05-09
Product CodeHNL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TSE-ANDERSON MODIFIED LACRIMAL GROOV is the device name listed in this FDA 510(k) record. The listed applicant is Hansen Ophthalmic Development Lab. It received FDA 510(k) clearance on 1984-05-09 under 510(k) number K840861. The device is classified under product code HNL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

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.

↑