MODEL 503FB— 510(k) K842759

Substantially Equivalent

Atrix

FDA 510(k) clearance K842759 for MODEL 503FB, Substantially Equivalent on 1985-01-18. Applicant: Atrix.

Clearance details

Applicant: Atrix
Product code: Product code LOS
Advisory panel: Unknown
Date received: 1984-07-16
Decision date: 1985-01-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Portland, OR, 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 Atrix

K852829 — CARDISUNY 501 A1986-02-26

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