FDA 510(k), K120917, HEADWAY DUO MICROCATHETER
FDA 510(k), K120917, HEADWAY DUO MICROCATHETER
510(K) Number: K120917
Device Name: HEADWAY DUO MICROCATHETER
Manufacturer: MICROVENTION, INC.
Device Classification Name: catheter, intravascular, diagnostic
Regulation Number: 870.1200
Classification Product Code: DQO
Date Received: 03/27/2012
Decision Date: 08/02/2012
Regulation Medical Specialty: Cardiovascular
Total pages: 293
Fully redacted pages: 193
Content pages: 100
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