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FDA 510(k)

LACRIMAL INTUBATION SET, DACRYOCYSTORHINOSTOMY (DCR) SET

K-Number: K990672 · 1999-05-18

ApplicantHurricane Medical
Decision Date1999-05-18
Product CodeOKS
DecisionSubstantially Equivalent

Device Summary

LACRIMAL INTUBATION SET, DACRYOCYSTORHINOSTOMY (DCR) SET is the device name listed in this FDA 510(k) record. The listed applicant is Hurricane Medical. It received FDA 510(k) clearance on 1999-05-18 under 510(k) number K990672. The device is classified under product code OKS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LACRIMAL INTUBATION SET, DACRYOCYSTORHINOSTOMY (DCR) SET?

LACRIMAL INTUBATION SET, DACRYOCYSTORHINOSTOMY (DCR) SET is a medical device that received FDA 510(k) clearance on 1999-05-18. The listed applicant is Hurricane Medical. The 510(k) number is K990672.

When did LACRIMAL INTUBATION SET, DACRYOCYSTORHINOSTOMY (DCR) SET receive FDA 510(k) clearance?

LACRIMAL INTUBATION SET, DACRYOCYSTORHINOSTOMY (DCR) SET received FDA 510(k) clearance on 1999-05-18, under 510(k) number K990672.

Who is the listed applicant for LACRIMAL INTUBATION SET, DACRYOCYSTORHINOSTOMY (DCR) SET?

The FDA 510(k) record lists Hurricane Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LACRIMAL INTUBATION SET, DACRYOCYSTORHINOSTOMY (DCR) SET?

The FDA product code for LACRIMAL INTUBATION SET, DACRYOCYSTORHINOSTOMY (DCR) SET 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.

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Other records listing Hurricane Medical 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.

K993361TUBING EXTENSION SETK990671DRAINAGE WICK; SURGICAL SPEARS AND SPONGES, CORNEAL LIGHT SHIELD, INSTRUMENT WIPE

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.

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