4,437 results
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45ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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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