ENSEMBLE CENTRAL STATION MONITOR— 510(k) K970358

Name: FDA 510(k) clearance K970358
Creator: U.S. Food and Drug Administration
Published: 1998-02-11

Substantially Equivalent

Mennen Medical, Inc.

FDA 510(k) clearance K970358 for ENSEMBLE CENTRAL STATION MONITOR, Substantially Equivalent on 1998-02-11. Applicant: Mennen Medical, Inc.. Device class: 2.

Clearance details

Applicant: Mennen Medical, Inc.
Product code: Code DSI
Device class: Class 2
Regulation: 21 CFR 870.1025
Advisory panel: Cardiovascular
Date received: 1997-01-30
Decision date: 1998-02-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rehovot, IL

Download summary PDF View on FDA.gov ↗

Recent devices under product code DSI

view all

K243349 — BodyGuardian Remote Monitoring System (BGRMS v3.0)2026-01-23
K250356 — MoMe ARC® Wireless Ambulatory ECG Monitoring and Detection System (32000)2025-07-29
K240177 — Zio AT® device (A100A1001)2024-10-30
K230265 — MoMe® ARC Wireless Ambulatory ECG Monitoring and Detection System2023-10-06
K231276 — SmartCardia 7L Platform2023-08-30

More clearances from Mennen Medical, Inc.

view all

K030722 — ENVOY PATIENT MONITOR2004-02-26
K983864 — ETCO2 VITAL SIGNS MODULE1999-10-08
K991775 — MODIFICATION TO COMPUTERIZED CATHETERIZATION LABORATORY - HORIZON 9000 WS1999-06-24
K982697 — MODIFICATION TO ENSEMBLE CENTRAL STATION MONITOR1998-08-12
K974510 — ENVOY PATIENT MONITOR1998-04-14

Adverse events under product code DSI

product code DSI

Death: 170
Injury: 729
Malfunction: 10,680
Total: 11,579

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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