TOENNIES NEUROSCREEN SYSTEM— 510(k) K972419

Substantially Equivalent

Erich Jaeger, Inc.

FDA 510(k) clearance K972419 for TOENNIES NEUROSCREEN SYSTEM, Substantially Equivalent on 1998-04-30. Applicant: Erich Jaeger, Inc.. Device class: 2.

Clearance details

Applicant: Erich Jaeger, Inc.
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 1997-06-27
Decision date: 1998-04-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hoechberg, Germany, DE

Download summary PDF View on FDA.gov ↗

Recent devices under product code IKN

K172743 — Natus VikingQuest2017-12-19
K163150 — ViMove22017-07-14
K162383 — Cadwell Sierra Summit, Cadwell Sierra Ascent2017-03-01
K142494 — ViMove2015-05-28
K131094 — VIMOVE2014-07-11

More clearances from Erich Jaeger, Inc.

K000396 — APNOESCREEN PRO, ALPHA SCREEN PRO2000-12-27
K960078 — ASTHMA MONITOR1996-09-20
K932744 — FLOWSCREEN1994-03-07
K933839 — MASTER SCREEN PNUEMO1994-03-07
K853443 — ALVEO-DIFFUSION TEST1986-02-21

Data sourced from openFDA. This site is unofficial and independent of the FDA.