435-0602.48; FFR v2.5

FDA registration

VOLCANO CORPORATION·1 product·🇺🇸 United States

435-0602.48; FFR v2.5

FDA registration

Volcano Corporation·1 product·🇺🇸 United States

FFR V2.5

FDA 510(k)

FDA Class 2 ·Radiology

EarQ

FDA UDI

Oticon A/S·05707131318602·G50, MRITE 312 2.4G NFM PB C094 EARQ

STERIS TOMOE SINGAPORE PTE LTD

FDA registration

STERIS TOMOE SINGAPORE PTE LTD·1 product·🇸🇬 Singapore

Infuset Flow Control Extension Set

FDA registration

EMED TECHNOLOGIES CORPORATION·1 product·🇺🇸 United States

CARDIO TECHNICS S.A. DE C.V.

FDA registration

CARDIO TECHNICS S.A. DE C.V.·1 product·🇲🇽 Mexico

INNOVATIVE MEDICAL MANUFACTURING CO.

FDA registration

INNOVATIVE MEDICAL MANUFACTURING CO.·1 product·🇹🇼 Taiwan

MyoCycle Pro

FDA registration

MYOLYN, INC·1 product·🇺🇸 United States

HA2 MEDIZINTECHNIK GMBH

FDA registration

HA2 MEDIZINTECHNIK GMBH·1 product·🇩🇪 Germany

AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING SOFTWARE, VERSION 3.1

FDA 510(k)

FDA Class 2 ·Cardiovascular

EMPIRA RX PTCA DILATATION CATHETER, EMPRIA NC RX PTCA DILATATION CATHETER

FDA 510(k)

FDA Class 2 ·Cardiovascular

Widex

FDA UDI

Widex A/S·05706069657630·Widex UNIQUE U-FP 330 DEMO (Winter silver ) Tel...

System, Imaging, Pulsed Echo, Ultrasonic

FDA classification

FDA Class 2 ·System, Imaging, Pulsed Echo, Ultrasonic

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA classification

FDA Class 2 ·Catheters, Transluminal Coronary Angioplasty, Percutaneous

Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

FDA classification

FDA Class 2 ·Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)