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FDA 510(k)

PARI VIOS

K-Number: K092918 · 2010-02-04

ApplicantPari Respiratory Equipment, Inc.
Decision Date2010-02-04
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PARI VIOS is the device name listed in this FDA 510(k) record. The listed applicant is Pari Respiratory Equipment, Inc.. It received FDA 510(k) clearance on 2010-02-04 under 510(k) number K092918. 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 PARI VIOS?

PARI VIOS is a medical device that received FDA 510(k) clearance on 2010-02-04. The listed applicant is Pari Respiratory Equipment, Inc.. The 510(k) number is K092918.

When did PARI VIOS receive FDA 510(k) clearance?

PARI VIOS received FDA 510(k) clearance on 2010-02-04, under 510(k) number K092918.

Who is the listed applicant for PARI VIOS?

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

What is the FDA product code for PARI VIOS?

The FDA product code for PARI VIOS is CAF.

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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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