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FDA 510(k)

NEBULIZER, DISP, 2D0815

K-Number: K780119 · 1978-04-03

ApplicantTravenol Laboratories, S.A.
Decision Date1978-04-03
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEBULIZER, DISP, 2D0815 is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1978-04-03 under 510(k) number K780119. 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 NEBULIZER, DISP, 2D0815?

NEBULIZER, DISP, 2D0815 is a medical device that received FDA 510(k) clearance on 1978-04-03. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K780119.

When did NEBULIZER, DISP, 2D0815 receive FDA 510(k) clearance?

NEBULIZER, DISP, 2D0815 received FDA 510(k) clearance on 1978-04-03, under 510(k) number K780119.

Who is the listed applicant for NEBULIZER, DISP, 2D0815?

The FDA 510(k) record lists Travenol Laboratories, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEBULIZER, DISP, 2D0815?

The FDA product code for NEBULIZER, DISP, 2D0815 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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