LungVision SmartWire Bridge
LungVision SmartWire Bridge (LV2055050), a bronchoscopic catheter (FDA Class II; FDA product code EOQ, Bronchoscope (Flexible Or Rigid)) made by Bodyvision Medical, Ltd., was cleared under FDA 510(k) K172955 on 26 Apr 2018 and listed in FDA GUDID on 13 Oct 2021 (UDI-DI 07290017652191); the registry lists it as not in commercial distribution (GUDID) 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 | Number07290017652191 | Date13 Oct 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK172955 | Date26 Apr 2018 | StatusActive |
Official records
- AccessGUDID record 07290017652191
- FDA 510(k) database K172955
Across registries
- FDA 510(k) K172955 decided 26 Apr 2018 Active
- FDA GUDID UDI-DI 07290017652191 listed 13 Oct 2021 Listed
Timeline
- Cleared FDA 510(k) K172955
- Listed FDA GUDID 07290017652191
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- LungVision SmartWire
- Generic name
- Bronchoscopic catheter
- Model / Ref / Catalog
- Bridge, LV2055050
- Primary DI / UDI-DI
- 07290017652191
- 510(k) Number
- FDA product code
- EOQ
- GMDN term
- Bronchoscopic catheter
- Device class
- Class II
- Regulation number
- 874.4680
- GUDID distribution status
- Not in Commercial Distribution
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