Launcher™ LA5LCB
Launcher™ LA5LCB is a Class II device made by Medtronic, Inc., cleared under FDA 510(k) K230156 on 30 Jun 2023 and listed in FDA GUDID since 12 May 2024 (UDI-DI 00763000900557), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00763000900557 | Date12 May 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK230156 | Date30 Jun 2023 | StatusActive |
Official records
- AccessGUDID record 00763000900557
- FDA 510(k) database K230156
Across registries
- FDA 510(k) K230156 decided 30 Jun 2023 Active
- FDA GUDID UDI-DI 00763000900557 listed 12 May 2024 Listed
Timeline
- Cleared FDA 510(k) K230156
- Listed FDA GUDID 00763000900557
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Launcher™
- Generic name
- Vascular guide-catheter, single-use
- Model / reference
- LA5LCB
- Primary DI / UDI-DI
- 00763000900557
- 510(k) Number
- FDA product code
- DQY
- GMDN term
- Vascular guide-catheter, single-use
- Device class
- Class II
- Regulation number
- 870.1250
- GUDID distribution status
- In Commercial Distribution
- Size
- Catheter Gauge — 5.0 FrenchLength — 100.0 Centimeter
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