Pathfinder SL 98000; 98200
by Spacelabs Healthcare (Washington), Inc 10 variants
Pathfinder SL 98000 +1 more model (040-1756-01) is a Class II device made by Spacelabs Healthcare (Washington), Inc, listed in FDA GUDID since 29 Jan 2019 (UDI-DI 10841522125904), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10841522125904 | Date29 Jan 2019 | StatusListed |
Official records
- AccessGUDID record 10841522125904
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Pathfinder SL
- Generic name
- Cardiology information system application software
- Model / Ref / Catalog
- 98000, 98200, 040-1756-01
- Primary DI / UDI-DI
- 10841522125904
- FDA product code
- DQK
- GMDN term
- Cardiology information system application software
- Models / Variants
- Device class
- Class II
- Regulation number
- 870.1425
- GUDID distribution status
- In Commercial Distribution
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