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: BSZ FDA class 2

Gas-Machine, Anesthesia

Anesthesiology

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The Gas-Machine, Anesthesia is a complex medical device that delivers precise and controlled mixtures of anesthetic gases and oxygen to a patient during surgical procedures, typically integrated with a ventilator and monitoring components. It is classified as FDA Class 2, requiring 510(k) premarket notification. The product code is BSZ, regulated under 21 CFR 868.5160 in the Anesthesiology specialty. This device is designated as life-sustaining or life-supporting.

510(k) Clearances

50+ matches
K Number
Device Name
Codonics Safe Labeling System-Point of Care Station (PCS) (SLS-700i and related 610i, 620i, 630i series enabled to retrofit RFID features); Codonics Safe Labeling System-Point of Care Station (PCS) (SLS-1, SLS XXX, Multiple Models Pending Configuration)
Atlan
Carestation 750/750c
A8, A9 Anesthesia System
Flow-i Anesthesia System, Flow-c Anesthesia System, Flow-e Anesthesia System
A5 Anesthesia System
A7 Anesthesia System
Aestiva 7900, Aestiva MRI, Aestiva 7100, Aestiva 7100 Compact, Aespire 100, Aespire 7100, Aespire 7900, Aespire View, Avance, Avance CS2, Aisys, Aisys CS2
Aisys CS2
FLOW-i Anesthesia System C20, FLOW-i Anesthesia System C30, FLOW-i Anesthesia System C40
Carestation 620/650/650C
A7 Anesthesia System
Aespire View
A7 Anesthesia System
MADM
DRE VENTURA
PERSEUS A500
A9800 ANESTHESIA WORKSTATION
FLOW-I ANESTHESIA SYSTEM C20, C30 & C40
GE DATEX-OHMEDA AISYS CS2 (AISYS CS^2)
GE DATEX-OHMEDA AVANCE CS2
INTELLISAVE AX700 ANESTHESIA SYSTEM
A5 ANESTHESIA DELIVERY SYSTEM
GE DATEX-OHMEDA AVANCE CS2
AESPIRE 7900, AESPIRE VIEW
MCKESSON ANESTHESIA CARE
SMARTPILOT VIEW MODEL MK04500
AM-6000 ANESTHESIA MACHINE
MAQUET FLOW-I C20, MAQUET FLOW-I C30, MAQUET FLOW-I C40
GE DATEX-OHMEDA AVANCE
GE DATEX-OHMEDA AISYS
NAVIGATOR APPLICATIONS SUITE
MAQUET FLOW-I C20, MAQUET FLOW-I C30, MODEL 66 77 200, 66 77 30
AS3700 ANESTHSIA DELIVERY SYSTEM
CODONICS SAFE LABELING SYSTEM (SLS), MODEL 500I/500P
AESPIRE 7900, AESPIRE VIEW
GE DATEX-OHMEDA S/5 ADU CARESTATION
NAVIGATOR APPLICATIONS SUITE
GE DATEX-OHMEDA AISYS
COMPURECORD PERI-OPERATIVE ANESTHESIOLOGY INFORMATION SYSTEM
FOURTH GAS MODULE WITH CO2 FOR PRIMUS US APOLLO
GE DATEX-OHMEDA AVANCE
NAVIGATOR APPLICATIONS SUITE
FABIUS MRI
NAVIGATOR ANESTHESIA DELIVERY SYSTEM, MODEL 0998-00-3024-01
GE DATEX-OHMEDA AISYS
MAGELLAN-2200, MODEL-3 ANESTHESIA MACHINE
NAVIGATOR APPLICATIONS SUITE
GE DATEX-OHMEDA AVANCE ANESTHESIA SYSTEM
ANESTHESIA INFORMATION AND DIGITAL-DRUG MANAGEMENT SYSTEM

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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