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GuideLiner Coast, 5.5F - GuideLiner Coast, 5.5F (5270)
FDA 510(k)Class II (US FDA 510(k))
510(k) K220647
Identifiers
- 510(k) Number
- K220647 FDA 510(k)
- FDA Product Code
- DQY FDA 510(k)
- Models / Variants
- GuideLiner Coast, 5.5F (5270) FDA 510(k)GuideLiner Coast, 6F (5271) FDA 510(k)GuideLiner Coast, 7F (5272) FDA 510(k)GuideLiner Coast, 8F (5273) FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 870.1250 FDA 510(k)
- Regulation Number
- 870.1250 FDA 510(k)
- Advisory Committee
- Cardiovascular FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
GuideLiner Coast, 5.5F - GuideLiner Coast, 5.5F (5270) by Vascular Solutions, LLC — Class II — FDA_510K — listed in FDA 510(k) — 4 models
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K220647 | Class II | Active |
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Manufacturer
- Manufacturer
- Vascular Solutions, LLC
Sources (1)
- FDA 510(k) K220647 24 fields · synced Jun 18, 2026