OXYCON PRO— 510(k) K992214

Substantially Equivalent

Erich Jaeger B.V.

FDA 510(k) clearance K992214 for OXYCON PRO, Substantially Equivalent on 2000-02-22. Applicant: Erich Jaeger B.V.. Device class: 2.

Clearance details

Applicant: Erich Jaeger B.V.
Product code: Code BZC
Device class: Class 2
Regulation: 21 CFR 868.1880
Advisory panel: Anesthesiology
Date received: 1999-07-01
Decision date: 2000-02-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nl-3981 La Bunnik, NL

Download summary PDF View on FDA.gov ↗

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More clearances from Erich Jaeger B.V.

K984465 — OXYCONALPHA WITH OPTION ECG1999-10-27
K980094 — MODIFICATION TO THE OXYCONALPHA1998-07-28

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