Cleared Traditional

K883732 - ARGIS PULMONARY FUNCTION TESTING SYSTEM

K883732 is an FDA 510(k) clearance for ARGIS PULMONARY FUNCTION TESTING SYSTEM, manufactured by Advanced Signal Processing, Inc.. The device is a Class 2 Anesthesiology device with product code BZC cleared through the Traditional 510(k) pathway after a 190-day FDA review.

K883732 · Advanced Signal Processing, Inc. · Anesthesiology device
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Mar 1989
Decision
190d
Days
Class 2
Risk

K883732 is an FDA 510(k) clearance for the ARGIS PULMONARY FUNCTION TESTING SYSTEM. Classified as Calculator, Pulmonary Function Data (product code BZC), Class II - Special Controls.

Submitted by Advanced Signal Processing, Inc. (Marietta, US). The FDA issued a Cleared decision on March 9, 1989 after a review of 190 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.1880 - the FDA anesthesiology and respiratory device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Anesthesiology review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K883732

510(k) Number K883732 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 31, 1988
Decision Date March 09, 1989
Days to Decision 190 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
50d slower than avg
Panel avg: 140d · This submission: 190d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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 59
Devices cleared under the same product code (BZC) and FDA review panel - the closest regulatory comparables to K883732.
PEDS WATER FILLED CATHETER/TRANSDUCER SYSTEM
K893845 · Medical Associated Services, Inc. · Oct 1989
OS-1 OCCLUSION SYSTEM - 1
K894839 · Medical, Inc. · Oct 1989
Q-PLEX 1
K881235 · Quinton, Inc. · Mar 1989
STAR CALC
K875027 · Infrasonics Corp. · Aug 1988
ALVEO-DIFFUSION TEST
K853443 · Erich Jaeger, Inc. · Feb 1986
OXYSCREEN
K843860 · Erich Jaeger, Inc. · Dec 1984
K883732 · ARGIS PULMONARY FUNCTION TESTING SYSTEM
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