139 results
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29ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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CLEARPOINT SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
MIX2VIAL TRANSFER DEVICE
FDA 510(k)
FDA Class 2
·General Hospital
MEDITECH MODEL ABPM-04
FDA 510(k)
FDA Class 2
·Cardiovascular
DERMOTHERAP GUN
FDA 510(k)
FDA Class 2
·General Hospital
A.B. DENTAL DEVICES
FDA 510(k)
FDA Class 2
·Dental
EpiFinder
FDA 510(k)
FDA Class 2
·General Hospital
IMPLASA-HOECHST GMBH IMPLANTS
FDA 510(k)
FDA Class 2
·Dental
HEARTTRENDS
FDA 510(k)
FDA Class 2
·Cardiovascular
NICOM
FDA 510(k)
FDA Class 2
·Cardiovascular
ENDOSCOUT
FDA 510(k)
FDA Class 2
·Radiology
IGI-SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
MAC 1600 ECG ANALYSIS SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
MULTLINK CABLE AND LEADWIRE SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
LOGIQ E9
FDA 510(k)
FDA Class 2
·Radiology
GE ECHOPAC
FDA 510(k)
FDA Class 2
·Radiology
REOSS POWDER, REOSS PUTTY, REOSS GEL, MODELS R-1,RP-1, RG-1
FDA 510(k)
FDA Class 2
·Orthopedic
Catheter, Electrode Recording, Or Probe, Electrode Recording
FDA Pre-Market Approval
FDA Class 2
·QWIKSTAR DIAGNOSTIC/ABLATION CATHETERS (MODELS D-1229 AND D-1230) AND QWIKSTAR INTERFACE CABLE (MODEL D-1195-12)
Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C Virus
FDA Pre-Market Approval
FDA Class 2
·AMPLICOR HCV TEST,VERSION 2.0
System, Nucleic Acid Amplification, Mycobacterium Tuberculosis Complex
FDA Pre-Market Approval
FDA Class 2
·AMPLICOR MYCOBACTERIUM TUBERCULOSIS (MTB) TEST
GE LOGIQ I COMAPACT ULTRASOUND, GE LOGIQ E COMPACT ULTRASOUND, GE VIVID E COMPACT ULTRASOUND
FDA 510(k)
FDA Class 2
·Radiology