AVD INTIMAX OCCLUSION CATHETER— 510(k) K910339
Substantially EquivalentApplied Vascular Devices, Inc.
FDA 510(k) clearance K910339 for AVD INTIMAX OCCLUSION CATHETER, Substantially Equivalent on 1991-05-29. Applicant: Applied Vascular Devices, Inc.. Device class: 2.
Clearance details
- Applicant
- Applied Vascular Devices, Inc.
- Product code
- Code DQT
- Device class
- Class 2
- Regulation
- 21 CFR 870.1370
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Laguna Hills, CA, US
Recent devices under product code DQT
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