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FDA 510(k)

VORTEX VALVED HOLDING CHAMBER

K-Number: K020944 · 2002-05-09

ApplicantPari Innovative Manufacturers, Inc.
Decision Date2002-05-09
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VORTEX VALVED HOLDING CHAMBER 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 2002-05-09 under 510(k) number K020944. 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 VORTEX VALVED HOLDING CHAMBER?

VORTEX VALVED HOLDING CHAMBER is a medical device that received FDA 510(k) clearance on 2002-05-09. The listed applicant is Pari Innovative Manufacturers, Inc.. The 510(k) number is K020944.

When did VORTEX VALVED HOLDING CHAMBER receive FDA 510(k) clearance?

VORTEX VALVED HOLDING CHAMBER received FDA 510(k) clearance on 2002-05-09, under 510(k) number K020944.

Who is the listed applicant for VORTEX VALVED HOLDING CHAMBER?

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 VORTEX VALVED HOLDING CHAMBER?

The FDA product code for VORTEX VALVED HOLDING CHAMBER 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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