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FDA 510(k)

XPERT NCT

K-Number: K941865 · 1994-09-29

ApplicantReichert Ophthalmic Instruments, Div. Leica, Inc.
Decision Date1994-09-29
Product CodeHKX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

XPERT NCT is the device name listed in this FDA 510(k) record. The listed applicant is Reichert Ophthalmic Instruments, Div. Leica, Inc.. It received FDA 510(k) clearance on 1994-09-29 under 510(k) number K941865. 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 XPERT NCT?

XPERT NCT is a medical device that received FDA 510(k) clearance on 1994-09-29. The listed applicant is Reichert Ophthalmic Instruments, Div. Leica, Inc.. The 510(k) number is K941865.

When did XPERT NCT receive FDA 510(k) clearance?

XPERT NCT received FDA 510(k) clearance on 1994-09-29, under 510(k) number K941865.

Who is the listed applicant for XPERT NCT?

The FDA 510(k) record lists Reichert Ophthalmic Instruments, Div. Leica, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for XPERT NCT?

The FDA product code for XPERT NCT is HKX.

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Other records listing Reichert Ophthalmic Instruments, Div. Leica, Inc. 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.

K000288REICHERT CT200 CONTACT TONOMETERK964290EYECHEK

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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