MATRX BATTERY CHARGER/DEFIBRILLATOR TESTER— 510(k) K895525

Name: FDA 510(k) clearance K895525
Creator: U.S. Food and Drug Administration
Published: 1990-01-26

Substantially Equivalent

Matrix Medica, Inc.

FDA 510(k) clearance K895525 for MATRX BATTERY CHARGER/DEFIBRILLATOR TESTER, Substantially Equivalent on 1990-01-26. Applicant: Matrix Medica, Inc.. Device class: 2.

Clearance details

Applicant: Matrix Medica, Inc.
Product code: Code DRL
Device class: Class 2
Regulation: 21 CFR 870.5325
Advisory panel: Cardiovascular
Date received: 1989-09-12
Decision date: 1990-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orchard Park, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DRL

view all

K190437 — Delta 33002019-08-28
K182905 — UniPulse2018-12-14
K153210 — Defibrillator Analyzer Variable Load2015-12-21
K110192 — DEFIBRILLATOR ANALYZER - DA-2006P2011-02-08
K083347 — IMPULSE 7010 DEFIBRILLATOR SELECTABLE LOADS2008-12-24

More clearances from Matrix Medica, Inc.

view all

K961536 — FLEXSCOPE1996-09-18
K923693 — KLORMAN1996-01-23
K921982 — MATRX HOPE(R) 5 RESUSCITATOR1994-10-28
K915353 — MATRX MEDICAL MAXIMIZER 1000 AND 2000 VACUUM PUMP1991-12-27
K912661 — MATRX, PYRAMID TRIANGLE BANDAGE1991-08-21

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