Medical Device Manufacturer · US , Minden , NV

Matrix Medica, Inc. - FDA 510(k) Cleared Devices

14 submissions · 13 cleared · Since 1985

Total

Cleared

Denied

Matrix Medica, Inc. has 13 FDA 510(k) cleared medical devices. Based in Minden, US.

Historical record: 13 cleared submissions from 1985 to 1996.

Browse the FDA 510(k) cleared devices submitted by Matrix Medica, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Matrix Medica, Inc.

14 devices

1-12 of 14

Cleared Sep 18, 1996

FLEXSCOPE

K961536 · GDB

Gastroenterology & Urology · 149d

Cleared Jan 23, 1996

KLORMAN

K923693 · LRJ

General Hospital · 1279d

Cleared Oct 28, 1994

MATRX HOPE(R) 5 RESUSCITATOR

K921982 · BTM

Anesthesiology · 913d

Cleared Dec 27, 1991

MATRX MEDICAL MAXIMIZER 1000 AND 2000 VACUUM PUMP

K915353 · EIA

Dental · 31d

Cleared Aug 21, 1991

MATRX, PYRAMID TRIANGLE BANDAGE

K912661 · ILI

Physical Medicine · 64d

Cleared May 09, 1990

MATRX DISPOSABLE NON-INVASIVE GELLED PACING ELEC.

K900551 · DRS

Cardiovascular · 92d

Cleared Jan 26, 1990

MATRX BATTERY CHARGER/DEFIBRILLATOR TESTER

K895525 · DRL

Cardiovascular · 136d

Cleared Jan 26, 1990

LIFE DEFENSE PLUS(TM), DEFIBRILLATOR/MONITOR/PACER

K895533 · LDD

Cardiovascular · 135d

NITRONOX(R), FIRST RESPONSE NITRONOX(TM)

K883833 · BZR

Anesthesiology · 161d

MITRAFLEX(TM) WOUND DRESSING

K873277 · NAD

General & Plastic Surgery · 31d

Matrix Medica, Inc. - FDA 510(k) Cleared Devices

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