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FDA 510(k)

NON-CONTACT TONOMETER, MODEL NT-4000

K-Number: K031733 · 2003-12-04

ApplicantNidek, Inc.
Decision Date2003-12-04
Product CodeHKX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

NON-CONTACT TONOMETER, MODEL NT-4000 is the device name listed in this FDA 510(k) record. The listed applicant is Nidek, Inc.. It received FDA 510(k) clearance on 2003-12-04 under 510(k) number K031733. 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 NON-CONTACT TONOMETER, MODEL NT-4000?

NON-CONTACT TONOMETER, MODEL NT-4000 is a medical device that received FDA 510(k) clearance on 2003-12-04. The listed applicant is Nidek, Inc.. The 510(k) number is K031733.

When did NON-CONTACT TONOMETER, MODEL NT-4000 receive FDA 510(k) clearance?

NON-CONTACT TONOMETER, MODEL NT-4000 received FDA 510(k) clearance on 2003-12-04, under 510(k) number K031733.

Who is the listed applicant for NON-CONTACT TONOMETER, MODEL NT-4000?

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

What is the FDA product code for NON-CONTACT TONOMETER, MODEL NT-4000?

The FDA product code for NON-CONTACT TONOMETER, MODEL NT-4000 is HKX.

Related Clinical Trials

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.

Other records listing Nidek, 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.

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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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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