KENZ-CARDICO 1201— 510(k) K870443

Substantially Equivalent

Suzuken Co., Ltd.

FDA 510(k) clearance K870443 for KENZ-CARDICO 1201, Substantially Equivalent on 1987-07-01. Applicant: Suzuken Co., Ltd..

Clearance details

Applicant: Suzuken Co., Ltd.
Product code: Code LOS
Advisory panel: Unknown
Date received: 1987-02-03
Decision date: 1987-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Culver City, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LOS

K090895 — EKG-PLUS II SOFTWARE2009-08-26
K083749 — CARDIOVIEW32 REVIEW MODULE2009-03-10
K073376 — PHILIPS ECG ALGORITHM2008-04-11
K023034 — CARDIOTOUCH-30002002-11-14
K011328 — CARDIO CARE EKG-2000 12-CHANNEL ELECTROCARDIOGRAPH2001-11-21

More clearances from Suzuken Co., Ltd.

K172068 — Kenz Cardico12112018-06-01
K101024 — KENZ CARDY302 MAX2011-01-06
K092389 — DISPOSAL ECG ELECTRODES, MODEL EASYRODE2009-10-13
K001896 — KENZ ECG 108 SINGLE CHANNEL DIGITAL ELECTROCARDIOGRAPHS; KENZ ECG 110 SINGLE CHANNEL DIGITAL ELECTROCARDIOGRAPHS WITH EC2001-01-08
K862544 — KENZ-ECG-102 SINGLE CHANNEL ELECTROCARDIOGRAPH1986-08-06

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