FDA 510(k), K061733, ANGIODYNAMICS SOFT-VU AND MARINER HYDROPHILIC COATED ANGIOGRAPHIC CATHETER
FDA 510(k), K061733, ANGIODYNAMICS SOFT-VU AND MARINER HYDROPHILIC COATED ANGIOGRAPHIC CATHETER
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510(K) Number: K061733
Device Name: ANGIODYNAMICS SOFT-VU AND MARINER HYDROPHILIC COATED ANGIOGRAPHIC CATHETER
Manufacturer: TERI JUCKETT
Device Classification Name: Catheter, Intravascular, Diagnostic
Regulation Number: DQO
Classification Product Code: 06/20/2006
Date Received: 08/24/2006
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: ANGIODYNAMICS SOFT-VU AND MARINER HYDROPHILIC COATED ANGIOGRAPHIC CATHETER
Manufacturer: TERI JUCKETT
Device Classification Name: Catheter, Intravascular, Diagnostic
Regulation Number: DQO
Classification Product Code: 06/20/2006
Date Received: 08/24/2006
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular