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FDA 510(k)

EFLOW ELECTRONIC INHALER/NEBULIZER

K-Number: K033833 · 2004-05-05

ApplicantPari Innovative Manufacturers, Inc.
Decision Date2004-05-05
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EFLOW ELECTRONIC INHALER/NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Pari Innovative Manufacturers, Inc.. It received FDA 510(k) clearance on 2004-05-05 under 510(k) number K033833. 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 EFLOW ELECTRONIC INHALER/NEBULIZER?

EFLOW ELECTRONIC INHALER/NEBULIZER is a medical device that received FDA 510(k) clearance on 2004-05-05. The listed applicant is Pari Innovative Manufacturers, Inc.. The 510(k) number is K033833.

When did EFLOW ELECTRONIC INHALER/NEBULIZER receive FDA 510(k) clearance?

EFLOW ELECTRONIC INHALER/NEBULIZER received FDA 510(k) clearance on 2004-05-05, under 510(k) number K033833.

Who is the listed applicant for EFLOW ELECTRONIC INHALER/NEBULIZER?

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

What is the FDA product code for EFLOW ELECTRONIC INHALER/NEBULIZER?

The FDA product code for EFLOW ELECTRONIC INHALER/NEBULIZER is CAF.

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Other records listing Pari Innovative Manufacturers, Inc. as applicant

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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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