587 results · 23ms · Sources: EU EUDAMED, US FDA

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval
FDA Class 2 ·AMERICAN EDWARDS LABS HYBRID PTCA CATHETER

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval
FDA Class 2 ·AMERICAN EDWARDS LABS HYBRID PTCA CATHETER

Lens, Contact (Other Material) - Daily

FDA Pre-Market Approval
FDA Class 2 ·OPTACRYL 60 (KOLFOCON A)RGP FINISHING LABS

TENS & EMS Device (LY-ET-01, LY-ET-02, LY-ET-04)

FDA 510(k)
FDA Class 2 ·Neurology

OmniTom Elite

FDA 510(k)
FDA Class 2 ·Radiology

BodyTom 64

FDA 510(k)
FDA Class 2 ·Radiology

OmniTom

FDA 510(k)
FDA Class 2 ·Radiology

NExCT 7

FDA 510(k)
FDA Class 2 ·Radiology

Tester, Pacemaker Electrode Function

FDA Pre-Market Approval
FDA Class 2 ·ATA SOFTWARE CARTRIDGE (SWM 1000 I-KTB.0.U)

Lens, Contact (Other Material) - Daily

FDA Pre-Market Approval
FDA Class 2 ·O-PERM F60 RGP CONTACT LENS ADD FINISH LABS

Lens, Contact (Other Material) - Daily

FDA Pre-Market Approval
FDA Class 2 ·OCUSIL(R) (NEFOCON A) CONTACT LENSES ADD FIN LABS

Lens, Contact (Other Material) - Daily

FDA Pre-Market Approval
FDA Class 2 ·O-PERM F60 RGP CONTACT LENS ADD FINISH LABS

Lens, Contact (Other Material) - Daily

FDA Pre-Market Approval
FDA Class 2 ·O-PERM F60 RGP CONTACT LENS ADD FINISH LABS

Lens, Contact (Other Material) - Daily

FDA Pre-Market Approval
FDA Class 2 ·OCUSIL(R) (NEFOCON A) CONTACT LENSES ADD FIN LABS

Lens, Contact (Other Material) - Daily

FDA Pre-Market Approval
FDA Class 2 ·OCUSIL(R) (NEFOCON A) CONTACT LENSES ADD FIN LABS

Lens, Contact (Other Material) - Daily

FDA Pre-Market Approval
FDA Class 2 ·O-PERM F60 RGP CONTACT LENS ADD FINISH LABS

Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C Virus

FDA Pre-Market Approval
FDA Class 2 ·VERSANT HCV RNA QUALITATIVE ASSAY/APTIMA HCV RNA QUALITATIVE ASSAY

System, Nucleic Acid Amplification, Mycobacterium Tuberculosis Complex

FDA Pre-Market Approval
FDA Class 2 ·AMPLIFIED MTD (MYCOBACTERIUM TUBERCULOSIS DIRECT) TEST

CPAP Cannulaide

FDA 510(k)
FDA Class 2 ·Anesthesiology

HAND HELD NEBULIZER SYSTEM

FDA 510(k)
FDA Class 2 ·Anesthesiology