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FDA 510(k)

PURITAN-BENNETT 700 RENAISSANCE II SPIROMETRY SYSTEM

K-Number: K022103 · 2002-09-27

ApplicantPuritan Bennett Corp.
Decision Date2002-09-27
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PURITAN-BENNETT 700 RENAISSANCE II SPIROMETRY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Puritan Bennett Corp.. It received FDA 510(k) clearance on 2002-09-27 under 510(k) number K022103. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PURITAN-BENNETT 700 RENAISSANCE II SPIROMETRY SYSTEM?

PURITAN-BENNETT 700 RENAISSANCE II SPIROMETRY SYSTEM is a medical device that received FDA 510(k) clearance on 2002-09-27. The listed applicant is Puritan Bennett Corp.. The 510(k) number is K022103.

When did PURITAN-BENNETT 700 RENAISSANCE II SPIROMETRY SYSTEM receive FDA 510(k) clearance?

PURITAN-BENNETT 700 RENAISSANCE II SPIROMETRY SYSTEM received FDA 510(k) clearance on 2002-09-27, under 510(k) number K022103.

Who is the listed applicant for PURITAN-BENNETT 700 RENAISSANCE II SPIROMETRY SYSTEM?

The FDA 510(k) record lists Puritan Bennett Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PURITAN-BENNETT 700 RENAISSANCE II SPIROMETRY SYSTEM?

The FDA product code for PURITAN-BENNETT 700 RENAISSANCE II SPIROMETRY SYSTEM is BZG.

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Related Devices (Code: BZG)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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