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FDA 510(k)

TONOMETER DIATON

K-Number: K060780 · 2006-04-06

ApplicantRyazan State Instruments
Decision Date2006-04-06
Product CodeHKX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TONOMETER DIATON is the device name listed in this FDA 510(k) record. The listed applicant is Ryazan State Instruments. It received FDA 510(k) clearance on 2006-04-06 under 510(k) number K060780. 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 TONOMETER DIATON?

TONOMETER DIATON is a medical device that received FDA 510(k) clearance on 2006-04-06. The listed applicant is Ryazan State Instruments. The 510(k) number is K060780.

When did TONOMETER DIATON receive FDA 510(k) clearance?

TONOMETER DIATON received FDA 510(k) clearance on 2006-04-06, under 510(k) number K060780.

Who is the listed applicant for TONOMETER DIATON?

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

What is the FDA product code for TONOMETER DIATON?

The FDA product code for TONOMETER DIATON 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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