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FDA 510(k)

(HEART) NEBULIZER

K-Number: K896696 · 1990-02-12

ApplicantVortran Medical Technology 1, Inc.
Decision Date1990-02-12
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

(HEART) NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Vortran Medical Technology 1, Inc.. It received FDA 510(k) clearance on 1990-02-12 under 510(k) number K896696. 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 (HEART) NEBULIZER?

(HEART) NEBULIZER is a medical device that received FDA 510(k) clearance on 1990-02-12. The listed applicant is Vortran Medical Technology 1, Inc.. The 510(k) number is K896696.

When did (HEART) NEBULIZER receive FDA 510(k) clearance?

(HEART) NEBULIZER received FDA 510(k) clearance on 1990-02-12, under 510(k) number K896696.

Who is the listed applicant for (HEART) NEBULIZER?

The FDA 510(k) record lists Vortran Medical Technology 1, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for (HEART) NEBULIZER?

The FDA product code for (HEART) NEBULIZER is CAF.

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Related Devices (Code: 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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