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FDA 510(k)

PARI PEP S

K-Number: K090829 · 2009-07-21

ApplicantPari Respiratory Equipment, Inc.
Decision Date2009-07-21
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PARI PEP S 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 2009-07-21 under 510(k) number K090829. The device is classified under product code BWF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARI PEP S?

PARI PEP S is a medical device that received FDA 510(k) clearance on 2009-07-21. The listed applicant is Pari Respiratory Equipment, Inc.. The 510(k) number is K090829.

When did PARI PEP S receive FDA 510(k) clearance?

PARI PEP S received FDA 510(k) clearance on 2009-07-21, under 510(k) number K090829.

Who is the listed applicant for PARI PEP S?

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 PEP S?

The FDA product code for PARI PEP S is BWF.

Other records listing Pari Respiratory Equipment, Inc. as applicant

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Related Devices (Code: BWF)

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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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