Revitalair 430F

FDA registration

OXAVITA S.R.L.·1 product·🇦🇷 Argentina

Revitalair 430F

FDA 510(k)

FDA Class 2 ·Anesthesiology

Chamber, Hyperbaric

FDA classification

FDA Class 2 ·Chamber, Hyperbaric

AbbottVasc (CR1) - ARMADA 35

FDA registration

Synergy Health AST, SRL·2 products·🇨🇷 Costa Rica

Armada 35/35LL PTA Catheter

FDA registration

Sterigenics Radiation Technologies, LLC·2 products·🇺🇸 United States

Armada 35 and 35LL Dilatation Catheters

FDA registration

Abbott Vascular·2 products·🇨🇷 Costa Rica

Armada 35 and 35LL Dilatation Catheters

FDA registration

Abbott Vascular Netherlands·2 products·🇳🇱 Netherlands

Armada 35 and 35LL Dilatation Catheters

FDA registration

ABBOTT VASCULAR·2 products·🇺🇸 United States

COMPASS HEALTH BRANDS (CORPORATE OFFICE)

FDA registration

COMPASS HEALTH BRANDS (CORPORATE OFFICE)·1 product·🇺🇸 United States

Armada 35 and 35LL Dilatation Catheters

FDA registration

ABBOTT VASCULAR·2 products·🇺🇸 United States

Shortwave diathermy therapeutic device

FDA registration

Shenzhen Dongdixin Technology Co., Ltd.·1 product·🇨🇳 China

FUSION GLO-TIP ERCP CATHETER

FDA registration

Wilson-Cook Medical Inc.·1 product·🇺🇸 United States

WiTouch Pro

FDA registration

HOLLYWOG, LLC·2 products·🇺🇸 United States

ARMADA 35/35LL PTA CATHETER

FDA 510(k)

FDA Class 2 ·Cardiovascular

BIS MODULE FOR ENVOY PATIENT MONITOR

FDA 510(k)

FDA Class 2 ·Neurology

Index-Generating Electroencephalograph Software

FDA classification

FDA Class 2 ·Index-Generating Electroencephalograph Software

Catheter, Angioplasty, Peripheral, Transluminal

FDA classification

FDA Class 2 ·Catheter, Angioplasty, Peripheral, Transluminal