Cleared Special

K072323 - MASTERSCREEN & OXYCON CPX

K072323 is an FDA 510(k) clearance for MASTERSCREEN & OXYCON CPX, manufactured by Viasys Healthcare GmbH. The device is a Class 2 Anesthesiology device with product code BZC cleared through the Special 510(k) pathway after a 51-day FDA review.

K072323 · Viasys Healthcare GmbH · Anesthesiology device
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Oct 2007
Decision
51d
Days
Class 2
Risk

K072323 is an FDA 510(k) clearance for the MASTERSCREEN & OXYCON CPX. Classified as Calculator, Pulmonary Function Data (product code BZC), Class II - Special Controls.

Submitted by Viasys Healthcare GmbH (Yorba Linda, US). The FDA issued a Cleared decision on October 10, 2007 after a review of 51 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.1880 - the FDA anesthesiology and respiratory device framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

FDA 510(k) Submission Details - K072323

510(k) Number K072323 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 20, 2007
Decision Date October 10, 2007
Days to Decision 51 days
Submission Type Special
Review Panel Anesthesiology (AN)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
89d faster than avg
Panel avg: 140d · This submission: 51d
Pathway characteristics
Modification to existing cleared device.

BZC Device Classification - Class 2, Special Controls

Product Code BZC Calculator, Pulmonary Function Data
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.1880
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 - BZC Calculator, Pulmonary Function Data

All 53
Devices cleared under the same product code (BZC) and FDA review panel - the closest regulatory comparables to K072323.
VYNTUS/ SENTRYSUITE PRODUCT LINE
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K052328 · Zan Messgerate GmbH · Dec 2005
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K023120 · Erich Jaeger GmbH · Nov 2003