OXYSCREEN— 510(k) K843860

Substantially Equivalent

Erich Jaeger, Inc.

FDA 510(k) clearance K843860 for OXYSCREEN, Substantially Equivalent on 1984-12-27. Applicant: Erich Jaeger, Inc.. Device class: 2.

Clearance details

Applicant: Erich Jaeger, Inc.
Product code: Code BZC
Device class: Class 2
Regulation: 21 CFR 868.1880
Advisory panel: Anesthesiology
Date received: 1984-10-01
Decision date: 1984-12-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Erich Jaeger, Inc.

K000396 — APNOESCREEN PRO, ALPHA SCREEN PRO2000-12-27
K972419 — TOENNIES NEUROSCREEN SYSTEM1998-04-30
K960078 — ASTHMA MONITOR1996-09-20
K932744 — FLOWSCREEN1994-03-07
K933839 — MASTER SCREEN PNUEMO1994-03-07

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