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)

OPAQUE HERRICK PLUG, 0.3MM; 0.5MM; O.7MM

K-Number: K001737 · 2000-06-19

ApplicantLacrimedics, Inc.
Decision Date2000-06-19
Product CodeLZU
DecisionSubstantially Equivalent

Device Summary

OPAQUE HERRICK PLUG, 0.3MM; 0.5MM; O.7MM is the device name listed in this FDA 510(k) record. The listed applicant is Lacrimedics, Inc.. It received FDA 510(k) clearance on 2000-06-19 under 510(k) number K001737. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPAQUE HERRICK PLUG, 0.3MM; 0.5MM; O.7MM?

OPAQUE HERRICK PLUG, 0.3MM; 0.5MM; O.7MM is a medical device that received FDA 510(k) clearance on 2000-06-19. The listed applicant is Lacrimedics, Inc.. The 510(k) number is K001737.

When did OPAQUE HERRICK PLUG, 0.3MM; 0.5MM; O.7MM receive FDA 510(k) clearance?

OPAQUE HERRICK PLUG, 0.3MM; 0.5MM; O.7MM received FDA 510(k) clearance on 2000-06-19, under 510(k) number K001737.

Who is the listed applicant for OPAQUE HERRICK PLUG, 0.3MM; 0.5MM; O.7MM?

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 OPAQUE HERRICK PLUG, 0.3MM; 0.5MM; O.7MM?

The FDA product code for OPAQUE HERRICK PLUG, 0.3MM; 0.5MM; O.7MM 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K161673LacriPro Punctum PlugK030300OPAQUE HERRICK LACRIMAL PLUGK021831OPAQUE HERRICK LACRIMAL PLUG, 0.3MM,0.5MM,0.7MM, MODELS HLP3-OPB,HLP50OPB,HLP7-OPBK963501HERRICK ULTIMATE PUNCTUM PLUGK963708HERRICK ULTIMATE PUNCTUM PLUGK944402FOCOMETER

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.

K241229Hello,eyes® BIO PlugBio Optics Co., Ltd.K222164Visant Medical Canalicular PlugVisant Medical, Inc.K213988SOFT PLUG Extended Duration 180 Tapered Canalicular PlugOasis Medical, Inc.K190210Tear Pool Dissolvable Punctum PlugsAlphamed, Inc.K162361Soft Plug Extended Duration 180 Canalicular PlugOasis Medical, Inc.K161673LacriPro Punctum PlugLacrimedics, Inc.

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.

↑