Cleared Abbreviated

K023225 - PURITAN BENNETT DATAFLOW DATA MANAGEMEN...

K023225 is an FDA 510(k) clearance for PURITAN BENNETT DATAFLOW DATA MANAGEMEN..., manufactured by Puritan Bennett Corp.. The device is a Class 2 Anesthesiology device with product code BZG cleared through the Abbreviated 510(k) pathway after a 82-day FDA review.

K023225 · Puritan Bennett Corp. · Anesthesiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 2002
Decision
82d
Days
Class 2
Risk

K023225 is an FDA 510(k) clearance for the PURITAN BENNETT DATAFLOW DATA MANAGEMENT SOFTWARE. Classified as Spirometer, Diagnostic (product code BZG), Class II - Special Controls.

Submitted by Puritan Bennett Corp. (Pleasanton, US). The FDA issued a Cleared decision on December 18, 2002 after a review of 82 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.1840 - the FDA anesthesiology and respiratory device framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Puritan Bennett Corp. devices

FDA 510(k) Submission Details - K023225

510(k) Number K023225 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 27, 2002
Decision Date December 18, 2002
Days to Decision 82 days
Submission Type Abbreviated
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
58d faster than avg
Panel avg: 140d · This submission: 82d
Pathway characteristics
Standards-based clearance path.

BZG Device Classification - Class 2, Special Controls

Product Code BZG Spirometer, Diagnostic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.1840
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Anesthesiology devices follow this clearance model.

Regulatory Peers - BZG Spirometer, Diagnostic

All 49
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