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FDA 510(k)

CANON FULL AUTO TONOMETER TX-F

K-Number: K023816 · 2002-11-26

ApplicantCanon, Inc.-Utsunomiya Optical Products Operation
Decision Date2002-11-26
Product CodeHKX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CANON FULL AUTO TONOMETER TX-F is the device name listed in this FDA 510(k) record. The listed applicant is Canon, Inc.-Utsunomiya Optical Products Operation. It received FDA 510(k) clearance on 2002-11-26 under 510(k) number K023816. The device is classified under product code HKX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANON FULL AUTO TONOMETER TX-F?

CANON FULL AUTO TONOMETER TX-F is a medical device that received FDA 510(k) clearance on 2002-11-26. The listed applicant is Canon, Inc.-Utsunomiya Optical Products Operation. The 510(k) number is K023816.

When did CANON FULL AUTO TONOMETER TX-F receive FDA 510(k) clearance?

CANON FULL AUTO TONOMETER TX-F received FDA 510(k) clearance on 2002-11-26, under 510(k) number K023816.

Who is the listed applicant for CANON FULL AUTO TONOMETER TX-F?

The FDA 510(k) record lists Canon, Inc.-Utsunomiya Optical Products Operation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CANON FULL AUTO TONOMETER TX-F?

The FDA product code for CANON FULL AUTO TONOMETER TX-F is HKX.

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Related Devices (Code: HKX)

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.

K253039AUTO KERATO-REFRACTO TONOMETER TRK-3 OMNIATopcon CorporationK223739VS Tabletop TonometerMedimaging Integrated Solution, Inc.K190382Intraocular Pressure Tonometer EASYTONCompany ElamedK181260MiiS Horus Scope DPT 100Medimaging Integrated Solution, Inc (Miis)K181143Keeler TonoCare TonometerKeeler Instruments, Inc.K180820Tono Vue Non-Contact TonometerCrystalvue Medical Corporation

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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