VASCULAR ARCHITECTS PERISCOPE DEVICE— 510(k) K003719
Substantially EquivalentVascular Architects, Inc.
FDA 510(k) clearance K003719 for VASCULAR ARCHITECTS PERISCOPE DEVICE, Substantially Equivalent on 2001-02-28. Applicant: Vascular Architects, Inc.. Device class: 2.
Clearance details
- Applicant
- Vascular Architects, Inc.
- Product code
- Code DWX
- Device class
- Class 2
- Regulation
- 21 CFR 870.4875
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Jose, CA, US
Recent devices under product code DWX
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- K012544 — VASCULAR ARCHITECTS ASPIRE COVERED STENT AND CONTROLLED EXPANSION DELIVERY SYSTEM
- K003173 — ASPIRE COVERED STENT AND DELIVERY CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.