Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: BZM FDA class 2

Calculator, Pulmonary Function Interpretor (Diagnostic)

Anesthesiology

View full classification →

The Calculator, Pulmonary Function Interpretor (Diagnostic) is a device that interprets pulmonary function test data and provides diagnostic conclusions or categorizations of lung function abnormalities to assist clinicians in clinical decision-making. It is classified as FDA Class 2, requiring 510(k) premarket notification. The product code is BZM, regulated under 21 CFR 868.1900 in the Anesthesiology specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

26 matches
K Number
Device Name
PULMOTRACK 2020 SYSTEM
PERSONAL WHEEZOMETER
WIM-PC, MODEL 1010
STG MULTICHANNEL LUNG SOUND ANALYSIS SYSTEM
PULMOTRACK,MODEL 1010
ORCA CARDIOPULMONARY EXERCISE TESTING SYSTEM
CPX, CCM, CATH WITH 15% CO2
MEDGRAPHICS EXERCISE CONSULT
PB100 DIAGNOSTIC SPIROMETER
EXERCISE EVALUATION SYSTEM 2010
BURROWS-KNUDSON AUTOMATED LUNG FUNCTION INTER. SYS
SINGLE BREATH LUNG DIFFUS TEST DEVICE SPIROMETERY
MEDICAL GRAPHICS DESKTOP DIAGNOSTIC SYSTEM
EXERSYSTEM(TM) MMC 5000
SPIROMETRICS MODEL 2500 FLOWMATE(TM)
SPIROVISION
PULMONARY FUNCTION TEST LABORATORY, SYSTEM 1070
SUPERSPIRO
UNIVERSAL COMPUTER INTERFACE SYSTEM
PHYSIOLOGICAL ANALYZER CM-710
CM-VII PHYSIOLOGIC ANALYZER
CDX 200
CARDIO-PULMONARY EXERCISE STRESS SYSTEM
PULMONARY LAB AUTOMATION SYSTEM
CYBER DX 100
SCREENING COMPUTEO SC-20

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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