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FDA 510(k)

OMRON ULTRASONIC NEBULIZER NE-U06

K-Number: K875134 · 1988-12-05

ApplicantNidek, Inc.
Decision Date1988-12-05
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OMRON ULTRASONIC NEBULIZER NE-U06 is the device name listed in this FDA 510(k) record. The listed applicant is Nidek, Inc.. It received FDA 510(k) clearance on 1988-12-05 under 510(k) number K875134. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OMRON ULTRASONIC NEBULIZER NE-U06?

OMRON ULTRASONIC NEBULIZER NE-U06 is a medical device that received FDA 510(k) clearance on 1988-12-05. The listed applicant is Nidek, Inc.. The 510(k) number is K875134.

When did OMRON ULTRASONIC NEBULIZER NE-U06 receive FDA 510(k) clearance?

OMRON ULTRASONIC NEBULIZER NE-U06 received FDA 510(k) clearance on 1988-12-05, under 510(k) number K875134.

Who is the listed applicant for OMRON ULTRASONIC NEBULIZER NE-U06?

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 OMRON ULTRASONIC NEBULIZER NE-U06?

The FDA product code for OMRON ULTRASONIC NEBULIZER NE-U06 is CAF.

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: CAF)

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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