MONITORING SYSTEM, MODEL ARGUS PB-2200— 510(k) K033738

Name: FDA 510(k) clearance K033738
Creator: U.S. Food and Drug Administration
Published: 2004-08-24

Substantially Equivalent

Schiller AG

FDA 510(k) clearance K033738 for MONITORING SYSTEM, MODEL ARGUS PB-2200, Substantially Equivalent on 2004-08-24. Applicant: Schiller AG. Device class: 2.

Clearance details

Applicant: Schiller AG
Product code: Code DSK
Device class: Class 2
Regulation: 21 CFR 870.1110
Advisory panel: Cardiovascular
Date received: 2003-11-28
Decision date: 2004-08-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Baar, CH

Download summary PDF View on FDA.gov ↗

Recent devices under product code DSK

view all

K231586 — Endophys Blood Pressure Monitor model BPM-302023-11-03
K160945 — Endophys Blood Pressure Monitor2016-09-26
K152582 — CORE FM System, Patient Interface Module (OPIM), Hemodynamic Converter Box2015-12-03
K141615 — ENDOPHYS BLOOD PRESSURE MONITOR2015-01-07
K080670 — MODIFICATION TO SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEM2008-04-23

More clearances from Schiller AG

view all

K253562 — medilogFD2026-08-14
K221056 — ARGUS PB-30002023-07-06
K183425 — CARDIOVIT AT-102 G22020-03-02
K170182 — CARDIOVIT FT-12017-07-19
K152043 — Diagnostic Station DS202016-05-06

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