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FDA 510(k)

MODIFICATION TO: EFLOW ELECTRONIC INHALER/NEBULIZER

K-Number: K072670 · 2007-12-13

ApplicantPari Innovative Manufacturers, Inc.
Decision Date2007-12-13
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO: 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 2007-12-13 under 510(k) number K072670. 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 MODIFICATION TO: EFLOW ELECTRONIC INHALER/NEBULIZER?

MODIFICATION TO: EFLOW ELECTRONIC INHALER/NEBULIZER is a medical device that received FDA 510(k) clearance on 2007-12-13. The listed applicant is Pari Innovative Manufacturers, Inc.. The 510(k) number is K072670.

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

MODIFICATION TO: EFLOW ELECTRONIC INHALER/NEBULIZER received FDA 510(k) clearance on 2007-12-13, under 510(k) number K072670.

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

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

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Related Devices (Code: CAF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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