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FDA 510(k)

MASTER SCREEN PNUEMO

K-Number: K933839 · 1994-03-07

ApplicantErich Jaeger, Inc.
Decision Date1994-03-07
Product CodeBTY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MASTER SCREEN PNUEMO is the device name listed in this FDA 510(k) record. The listed applicant is Erich Jaeger, Inc.. It received FDA 510(k) clearance on 1994-03-07 under 510(k) number K933839. The device is classified under product code BTY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASTER SCREEN PNUEMO?

MASTER SCREEN PNUEMO is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is Erich Jaeger, Inc.. The 510(k) number is K933839.

When did MASTER SCREEN PNUEMO receive FDA 510(k) clearance?

MASTER SCREEN PNUEMO received FDA 510(k) clearance on 1994-03-07, under 510(k) number K933839.

Who is the listed applicant for MASTER SCREEN PNUEMO?

The FDA 510(k) record lists Erich Jaeger, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MASTER SCREEN PNUEMO?

The FDA product code for MASTER SCREEN PNUEMO is BTY.

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Other records listing Erich Jaeger, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K000396APNOESCREEN PRO, ALPHA SCREEN PROK972419TOENNIES NEUROSCREEN SYSTEMK960078ASTHMA MONITORK932744FLOWSCREENK853443ALVEO-DIFFUSION TESTK853434ERGO-PNEUMOTEST

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Related Devices (Code: BTY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260242CPETWise PlatformMedibyt , Ltd.K242809Ascent Cardiorespiratory Diagnostic SoftwareMedical Graphics CorporationK223629SpiroSphere, SpiroSphereECG, CardioSphereEresearchtechnology GmbHK231561Pulmonary Function Tester, Model: A9Guangzhou Homesun Medical Technology Co., Ltd.K222982Virtus Metabolic MonitorVirtus Technology ApsK221030Model 9100 PFT/DICOVitalograph Ireland, Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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