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KOI LACREMAL HOOK & DILATOR — Koi, Inc. (510(k) K812097)

KOI LACREMAL HOOK & DILATOR — Koi, Inc. (510(k) K812097) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: KOI LACREMAL HOOK & DILATOR; Applicant: Koi, Inc.; Clearance track: 510(k).

Device nameKOI LACREMAL HOOK & DILATOR
ApplicantKoi, Inc.
Clearance track510(k)
Submission numberK812097
DecisionSubstantially Equivalent
Decision date1981-08-18
Date received1981-07-24
Product codeHNW
Device class1
Medical specialtyOphthalmic
Applicant locationIL, US
SourceopenFDA device

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