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FDA 510(k)

LACRIFAST

K-Number: K120886 · 2012-12-17

ApplicantHiroyasu Higuchi
Decision Date2012-12-17
Product CodeOKS
DecisionSubstantially Equivalent

Device Summary

LACRIFAST is the device name listed in this FDA 510(k) record. The listed applicant is Hiroyasu Higuchi. It received FDA 510(k) clearance on 2012-12-17 under 510(k) number K120886. The device is classified under product code OKS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LACRIFAST?

LACRIFAST is a medical device that received FDA 510(k) clearance on 2012-12-17. The listed applicant is Hiroyasu Higuchi. The 510(k) number is K120886.

When did LACRIFAST receive FDA 510(k) clearance?

LACRIFAST received FDA 510(k) clearance on 2012-12-17, under 510(k) number K120886.

Who is the listed applicant for LACRIFAST?

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

What is the FDA product code for LACRIFAST?

The FDA product code for LACRIFAST is OKS.

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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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