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FDA 510(k)

VITAL COUGH

K-Number: K120277 · 2012-09-12

ApplicantLung Assist, Inc.
Decision Date2012-09-12
Product CodeNHJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VITAL COUGH is the device name listed in this FDA 510(k) record. The listed applicant is Lung Assist, Inc.. It received FDA 510(k) clearance on 2012-09-12 under 510(k) number K120277. The device is classified under product code NHJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITAL COUGH?

VITAL COUGH is a medical device that received FDA 510(k) clearance on 2012-09-12. The listed applicant is Lung Assist, Inc.. The 510(k) number is K120277.

When did VITAL COUGH receive FDA 510(k) clearance?

VITAL COUGH received FDA 510(k) clearance on 2012-09-12, under 510(k) number K120277.

Who is the listed applicant for VITAL COUGH?

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

What is the FDA product code for VITAL COUGH?

The FDA product code for VITAL COUGH is NHJ.

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Related Devices (Code: NHJ)

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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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