4,437 results · 45ms · Sources: EU EUDAMED, US FDA

Electroporation System (N3000)

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

ONCOBIONIC SYSTEM

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Irreversible Electroporation Ablation Generator, Irreversible Electroporation Probe

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

NanoKnife Generator (H78720300301US0); NanoKnife Single Electrode Activation Probe, 15 cm (H787204001090); NanoKnife Single Electrode Activation Probe, 25 cm (H787204001100); NanoKnife Single Electrode Probe Spacer (H787204003010)

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

NanoKnife System

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

ONCOBIONIC SYSTEM

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Canady Helios Cold Plasma™ XL-1000CP™ Ablation System (XL-1000CPSYS)

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

NanoKnife System

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

THE STORK OTC

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

AFIAS TSH-SP, AFIAS TSH-VB, AFIAS-6/SP Analyzer, AFIAS-6/VB Analyzer

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

Wearable Breast Pump (ABP-1508PRO, ABP-1506, ABP-1306, ABP-1306 PRO, M1, M3, M8, M5, M6, K1, K2, K3, K5, ABP-1306PLUS, ABP-1308, M2)

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

Smart double sides wearable breast pump, Electric bilateral breast pump

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

Pulse Generator, External Pacemaker, Dual Chamber

FDA Pre-Market Approval
FDA Class 2 ·REOCOR S / D FAMILY OF EXTERNAL PACEMAKERS

Pulse Generator, External Pacemaker, Dual Chamber

FDA Pre-Market Approval
FDA Class 2 ·RELIATY / MODEL 3145 FAMILY OF PACING SYSTEM ANALYZERS

Pulse Generator, External Pacemaker, Dual Chamber

FDA Pre-Market Approval
FDA Class 2 ·RELIATY / MODEL 3145 PACING SYSTEM

HEARTSTART 2000, MANUAL DEFIBRILLATOR

FDA 510(k)
FDA Class 2 ·Cardiovascular

AIR-CUSHION TOCOTONOMETER

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

FETASCAN 1500

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

FIRST MEDIC MODEL 610P

FDA 510(k)
FDA Class 2 ·Cardiovascular

HEARTSTART 2000 DEFIBRILLATOR TESTER, ECG

FDA 510(k)
FDA Class 2 ·Cardiovascular