377 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·SPECTRAPROBE-PLR MODEL 900 OPTILASE CONTACT LASER
Device. Laser Peripheral Angioplasty
FDA Pre-Market Approval
FDA Class 3
·TRIMEDYNE'S LASERPROBE-PLR{TM} CATHETER & OPTILASE
Device. Laser Peripheral Angioplasty
FDA Pre-Market Approval
FDA Class 3
·TRIMEDYNE'S LASERPROBE-PLR{TM} CATHETER & OPTILASE
Device. Laser Peripheral Angioplasty
FDA Pre-Market Approval
FDA Class 3
·TRIMEDYNE'S LASERPROBE-PLR{TM} CATHETER & OPTILASE
Device. Laser Peripheral Angioplasty
FDA Pre-Market Approval
FDA Class 3
·TRIMEDYNE'S LASERPROBE-PLR{TM} CATHETER & OPTILASE
Device. Laser Peripheral Angioplasty
FDA Pre-Market Approval
FDA Class 3
·TRIMEDYNE'S LASERPROBE-PLR{TM} CATHETER & OPTILASE
Device. Laser Peripheral Angioplasty
FDA Pre-Market Approval
FDA Class 3
·TRIMEDYNE'S LASERPROBE-PLR{TM} CATHETER & OPTILASE
Device. Laser Peripheral Angioplasty
FDA Pre-Market Approval
FDA Class 3
·TRIMEDYNE'S LASERPROBE-PLR{TM} CATHETER & OPTILASE
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VENTAK(R) P3 AICD(TM) SYSTEM
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·8 ECTRAPROBE-PLR MODEL 900 OPTILASE CONTACT LASER
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·8 ECTRAPROBE-PLR MODEL 900 OPTILASE CONTACT LASER
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·8 ECTRAPROBE-PLR MODEL 900 OPTILASE CONTACT LASER
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·8 ECTRAPROBE-PLR MODEL 900 OPTILASE CONTACT LASER
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·8 ECTRAPROBE-PLR MODEL 900 OPTILASE CONTACT LASER
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·8 ECTRAPROBE-PLR MODEL 900 OPTILASE CONTACT LASER
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·8 ECTRAPROBE-PLR MODEL 900 OPTILASE CONTACT LASER
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·8 ECTRAPROBE-PLR MODEL 900 OPTILASE CONTACT LASER
PERMACOL SURGICAL IMPLANT T-PIECE, PERMACOL SURGICAL IMPLANT RECTOCELE-PIECE, MODELS 5928-150, 5645-150
FDA 510(k)
FDA Class 3
·Obstetrics/Gynecology
Pump, Infusion, Implanted, Programmable
FDA Pre-Market Approval
FDA Class 3
·CODMAN 3000 SERIES IMPLANTABLE INFUSION PUMP.
Tissue Adhesive Internal Use
FDA Pre-Market Approval
FDA Class 3
·LIQUIFIX FIX8 Laparoscopic Hernia Mesh Fixation Device, LIQUIFIX Precision Open Hernia Mesh Fixation Device