LungVision Tool Bridge
by Bodyvision Medical, Ltd. 12 variants
LungVision Tool Bridge (LV2055004) is a bronchoscopic catheter (FDA Class II; FDA product code EOQ, Bronchoscope (Flexible Or Rigid)) made by Bodyvision Medical, Ltd., cleared under FDA 510(k) K172955 on 26 Apr 2018 and listed in FDA GUDID since 1 Jan 2020 (UDI-DI 07290017652061), 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 | Number07290017652061 | Date1 Jan 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK172955 | Date26 Apr 2018 | StatusActive |
Official records
- AccessGUDID record 07290017652061
- FDA 510(k) database K172955
Across registries
- FDA 510(k) K172955 decided 26 Apr 2018 Active
- FDA GUDID UDI-DI 07290017652061 listed 1 Jan 2020 Listed
Timeline
- Cleared FDA 510(k) K172955
- Listed FDA GUDID 07290017652061
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- LungVision Tool
- Generic name
- Bronchoscopic catheter
- Model / Ref / Catalog
- Bridge, LV2055004
- Primary DI / UDI-DI
- 07290017652061
- 510(k) Number
- FDA product code
- EOQ
- GMDN term
- Bronchoscopic catheter
- Device class
- Class II
- Regulation number
- 874.4680
- GUDID distribution status
- In Commercial Distribution
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