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FDA 510(k)

VORTRAN INTERMITTENT SIGNAL ACTIVATED NEBULIZER

K-Number: K911759 · 1991-09-10

ApplicantVortran Medical Technology 1, Inc.
Decision Date1991-09-10
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VORTRAN INTERMITTENT SIGNAL ACTIVATED 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 1991-09-10 under 510(k) number K911759. 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 VORTRAN INTERMITTENT SIGNAL ACTIVATED NEBULIZER?

VORTRAN INTERMITTENT SIGNAL ACTIVATED NEBULIZER is a medical device that received FDA 510(k) clearance on 1991-09-10. The listed applicant is Vortran Medical Technology 1, Inc.. The 510(k) number is K911759.

When did VORTRAN INTERMITTENT SIGNAL ACTIVATED NEBULIZER receive FDA 510(k) clearance?

VORTRAN INTERMITTENT SIGNAL ACTIVATED NEBULIZER received FDA 510(k) clearance on 1991-09-10, under 510(k) number K911759.

Who is the listed applicant for VORTRAN INTERMITTENT SIGNAL ACTIVATED 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 VORTRAN INTERMITTENT SIGNAL ACTIVATED NEBULIZER?

The FDA product code for VORTRAN INTERMITTENT SIGNAL ACTIVATED 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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