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FDA 510(k)

FPT NEBULIZER

K-Number: K970010 · 1997-04-01

ApplicantFluid Propulsion Technologies, Inc.
Decision Date1997-04-01
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FPT NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Fluid Propulsion Technologies, Inc.. It received FDA 510(k) clearance on 1997-04-01 under 510(k) number K970010. 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 FPT NEBULIZER?

FPT NEBULIZER is a medical device that received FDA 510(k) clearance on 1997-04-01. The listed applicant is Fluid Propulsion Technologies, Inc.. The 510(k) number is K970010.

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

FPT NEBULIZER received FDA 510(k) clearance on 1997-04-01, under 510(k) number K970010.

Who is the listed applicant for FPT NEBULIZER?

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

What is the FDA product code for FPT NEBULIZER?

The FDA product code for FPT NEBULIZER is CAF.

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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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