Medical Device Manufacturer · US , Raynham , MA

Johnson & Johnson Professionals, Inc. - FDA 510(k) Cleared Devices

206 submissions · 184 cleared · Since 1976

Official Website

206

Total

184

Cleared

0

Denied

FDA 510(k) Regulatory Record - Johnson & Johnson Professionals, Inc. Cardiovascular ✕

9 devices

1-9 of 9

Cleared Nov 06, 1987

MAXIMA* COLLAPSIBLE VENOUS RESERVOIR BAG & HOLDER

Cardiovascular · 73d

Cleared Feb 19, 1987

INTERSEPT* CARDIOTOMY RESERVOIR WITH FILTER

Cardiovascular · 66d

Cleared Jan 02, 1987

ARTERIAL 20/40 MICRON FILTERS W/WO HEPARIN COATING

Cardiovascular · 65d

Cleared Jul 24, 1986

MERIDIAN IMAGING SYSTEM

Cardiovascular · 79d

Cleared Jul 09, 1986

MODEL UST-SSD 880L1-5 TRANESOPHAGEAL PHASED ARRAY

Cardiovascular · 65d

Cleared Apr 14, 1986

ULTRASONIC COUPLANT GEL

Cardiovascular · 123d

Cleared Feb 21, 1986

MERIDIAN ULTRASOUND IMAGING SYSTEM

Cardiovascular · 204d

Cleared Oct 16, 1985

J & J CARDIOVASCULAR MAXIMA HOLLOW FIBER OXYGENATO

Cardiovascular · 79d

Cleared Apr 05, 1977

Cardiovascular · 32d