FDA 510(k)

N20 TEST

K-Number: K853360 · 1985-09-03

Decision Date1985-09-03

Product CodeCBR

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

N20 TEST 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 1985-09-03 under 510(k) number K853360. The device is classified under product code CBR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the N20 TEST?

N20 TEST is a medical device that received FDA 510(k) clearance on 1985-09-03. The listed applicant is Erich Jaeger, Inc.. The 510(k) number is K853360.

When did N20 TEST receive FDA 510(k) clearance?

N20 TEST received FDA 510(k) clearance on 1985-09-03, under 510(k) number K853360.

Who is the listed applicant for N20 TEST?

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 N20 TEST?

The FDA product code for N20 TEST is CBR.

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 PRO K972419TOENNIES NEUROSCREEN SYSTEM K960078ASTHMA MONITOR K932744FLOWSCREEN K933839MASTER SCREEN PNUEMO K853443ALVEO-DIFFUSION TEST

View all 28 devices →

Related Devices (Code: CBR)

K112173SPEACELABS MULTIGAS MODULESpacelabs Healthcare K053599SPACELABS MEDICAL MULTIGAS ANALYZER MODULE 91518 AND ACCESSORIESSpacelabs Medical, Inc.K954962SPACELABS MEDICAL MULTIGAS ANALYZERSpacelabs, Inc.K904843OSCAR(TM) II CAPNOMETER & PULSE OXIMETERDalton Instrument Corp.

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.