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FDA 510(k)

ULTRASONIC NEBULIZER SYSTEM, MODEL KN-9210

K-Number: K083256 · 2009-06-26

ApplicantK-Jump Health Co., Ltd.
Decision Date2009-06-26
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ULTRASONIC NEBULIZER SYSTEM, MODEL KN-9210 is the device name listed in this FDA 510(k) record. The listed applicant is K-Jump Health Co., Ltd.. It received FDA 510(k) clearance on 2009-06-26 under 510(k) number K083256. 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 ULTRASONIC NEBULIZER SYSTEM, MODEL KN-9210?

ULTRASONIC NEBULIZER SYSTEM, MODEL KN-9210 is a medical device that received FDA 510(k) clearance on 2009-06-26. The listed applicant is K-Jump Health Co., Ltd.. The 510(k) number is K083256.

When did ULTRASONIC NEBULIZER SYSTEM, MODEL KN-9210 receive FDA 510(k) clearance?

ULTRASONIC NEBULIZER SYSTEM, MODEL KN-9210 received FDA 510(k) clearance on 2009-06-26, under 510(k) number K083256.

Who is the listed applicant for ULTRASONIC NEBULIZER SYSTEM, MODEL KN-9210?

The FDA 510(k) record lists K-Jump Health Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTRASONIC NEBULIZER SYSTEM, MODEL KN-9210?

The FDA product code for ULTRASONIC NEBULIZER SYSTEM, MODEL KN-9210 is CAF.

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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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