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FDA 510(k)

PURITAN BENNETT DATAFLOW DATA MANAGEMENT SOFTWARE

K-Number: K023225 · 2002-12-18

ApplicantPuritan Bennett Corp.
Decision Date2002-12-18
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PURITAN BENNETT DATAFLOW DATA MANAGEMENT SOFTWARE 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 2002-12-18 under 510(k) number K023225. 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 DATAFLOW DATA MANAGEMENT SOFTWARE?

PURITAN BENNETT DATAFLOW DATA MANAGEMENT SOFTWARE is a medical device that received FDA 510(k) clearance on 2002-12-18. The listed applicant is Puritan Bennett Corp.. The 510(k) number is K023225.

When did PURITAN BENNETT DATAFLOW DATA MANAGEMENT SOFTWARE receive FDA 510(k) clearance?

PURITAN BENNETT DATAFLOW DATA MANAGEMENT SOFTWARE received FDA 510(k) clearance on 2002-12-18, under 510(k) number K023225.

Who is the listed applicant for PURITAN BENNETT DATAFLOW DATA MANAGEMENT SOFTWARE?

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 DATAFLOW DATA MANAGEMENT SOFTWARE?

The FDA product code for PURITAN BENNETT DATAFLOW DATA MANAGEMENT SOFTWARE is BZG.

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Other records listing Puritan Bennett Corp. as applicant

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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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