Identity
- Trade Name
- SuperCross™ FT microcatheter FDA UDI
- Generic Name
- Peripheral vascular intervention infusion catheter FDA UDI
- Device Name
- The SuperCross microcatheter is intended to be used in conjunction with steerable guidewires to access discrete regions of the coronary and/or peripheral vasculature. It may be used to facilitate placement and exchange of guidewires and other interventional devices and to subselectively infuse/deliver diagnostic and therapeutic agents. FDA UDI
- Model / Reference
- 5341 FDA UDI
- Description
- The SuperCross microcatheter is intended to be used in conjunction with steerable guidewires to access discrete regions of the coronary and/or peripheral vasculature. It may be used to facilitate placement and exchange of guidewires and other interventional devices and to subselectively infuse/deliver diagnostic and therapeutic agents. FDA UDI
Identifiers
- Primary DI / UDI-DI
- M20653410 FDA UDI
- 510(k) Number
- K101659 FDA UDI
- FDA Product Code
- DQY FDA UDI
- GMDN Term
- Peripheral vascular intervention infusion catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1250 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 150 Centimeter FDA UDI
Category: Peripheral vascular intervention infusion catheter
SuperCross™ FT microcatheter by Vascular Solutions, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K101659 also covers:
- SUPERCROSS — TELEFLEX INCORPORATED
- SUPERCROSS — TELEFLEX INCORPORATED
- SUPERCROSS — TELEFLEX INCORPORATED
- SUPERCROSS — TELEFLEX INCORPORATED
- SUPERCROSS — TELEFLEX INCORPORATED
- SUPERCROSS — TELEFLEX INCORPORATED
- SUPERCROSS — TELEFLEX INCORPORATED
- SUPERCROSS — TELEFLEX INCORPORATED
- SUPERCROSS — TELEFLEX INCORPORATED
- SUPERCROSS — TELEFLEX INCORPORATED
- SUPERCROSS — TELEFLEX INCORPORATED
- SUPERCROSS — TELEFLEX INCORPORATED
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Vascular Solutions, Inc.
Sources (1)
- FDA UDI 2699a3d9-937f-4d0f-84b7-ad2fd826deae 36 fields · synced May 30, 2026