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)

BECKER TRANSNASAL LACRIMAL (INTUBATION SETS)

K-Number: K023758 · 2003-09-17

ApplicantFci Ophthalmics, Inc.
Decision Date2003-09-17
Product CodeOKS
DecisionSubstantially Equivalent

Device Summary

BECKER TRANSNASAL LACRIMAL (INTUBATION SETS) is the device name listed in this FDA 510(k) record. The listed applicant is Fci Ophthalmics, Inc.. It received FDA 510(k) clearance on 2003-09-17 under 510(k) number K023758. The device is classified under product code OKS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BECKER TRANSNASAL LACRIMAL (INTUBATION SETS)?

BECKER TRANSNASAL LACRIMAL (INTUBATION SETS) is a medical device that received FDA 510(k) clearance on 2003-09-17. The listed applicant is Fci Ophthalmics, Inc.. The 510(k) number is K023758.

When did BECKER TRANSNASAL LACRIMAL (INTUBATION SETS) receive FDA 510(k) clearance?

BECKER TRANSNASAL LACRIMAL (INTUBATION SETS) received FDA 510(k) clearance on 2003-09-17, under 510(k) number K023758.

Who is the listed applicant for BECKER TRANSNASAL LACRIMAL (INTUBATION SETS)?

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

What is the FDA product code for BECKER TRANSNASAL LACRIMAL (INTUBATION SETS)?

The FDA product code for BECKER TRANSNASAL LACRIMAL (INTUBATION SETS) is OKS.

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 Fci Ophthalmics, 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.

K061404MONO-CRAWFORD NASO-LACRIMAL INTUBATION DEVICEK061398SNUG PLUG PUNCTUM PLUGK041869SELF RETAINING BICANALICULUS INTUBATION SETK023400FCI MESH WRAPPED BIOCERAMIC ORBITAL IMPLANTK030054DISPOSABLE VITRECTOMY SETS, DISPOSABLE VIRECTOMY LENSESK992294BIOCERAMIC ORBITAL IMPLANT

View all 13 devices →

Related Devices (Code: OKS)

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.

K201892Ritleng®+ and Ritleng®+ PVPFci (France Chirurgie Instrumentation) SasK201606LacriJet®Fci (France Chirurgie Instrumentation) SasK170247Lacriflow CLKaneka Pharma America, LLCK161373NunchakuFci (France Chirurgie Instrumentation)K160710Oasis Lacrimal Intubation SetAnodyneK130375SELF-RETAINING BICANALICULUS INTUBATON SET IIFci Sas (France Chirurgie Instrumentation)

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.

↑