VASCULAR SOLUTIONS DUETT MODEL 1000 SEALING DEVICE
FDA premarket approval P990037/S002 · decided 2001-03-14
Approval details
- PMA number
- P990037
- Supplement
- S002
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- VASCULAR SOLUTIONS DUETT MODEL 1000 SEALING DEVICE
- Applicant
- Vascular Solutions, Inc.
- Date received
- 2001-01-22
- Decision date
- 2001-03-14
- Days to decision
- 51 days
- Decision code
- APPR
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Minneapolis, MN
- Statement
- APPROVAL FOR CHANGES TO THE INSTRUCTIONS FOR USE MANUAL.
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510(k) clearances by this applicant
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|---|---|---|
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| TrapLiner catheter (K180088) | Vascular Solutions, Inc. | 2018-04-04 |
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| Gel-Bead (600-800 micron) - 1 ml sphere volume, Gel-Bead (600-800 micron) - 2 ml sphere volume (K173891) | Vascular Solutions, Inc. | 2018-01-19 |
| Raider Guidewire (K173532) | Vascular Solutions, Inc. | 2017-12-15 |
| Octane aspiration system (K173266) | Vascular Solutions, Inc. | 2017-12-01 |