CorPath GRX Drape, Control Console 311
CorPath GRX Drape, Control Console 311 is a Class II device made by Corindus, Inc., cleared under FDA 510(k) K202275 on 11 Dec 2020 (2 earlier submissions) and listed in FDA GUDID since 20 Jan 2017 (UDI-DI 00816280023116), active (FDA 510(k)), not in commercial distribution (GUDID) as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK202275 | Date11 Dec 2020 | StatusActive |
| United States | GUDID listing | Number00816280023116 | Date20 Jan 2017 | StatusListed |
Official records
- AccessGUDID record 00816280023116
- FDA 510(k) database K202275
- FDA 510(k) database K173288
- FDA 510(k) database K160121
Across registries
- FDA 510(k) K202275 decided 11 Dec 2020 Active
- FDA GUDID UDI-DI 00816280023116 listed 20 Jan 2017 Listed
Timeline
- Cleared FDA 510(k) K160121
- Listed FDA GUDID 00816280023116
- Cleared FDA 510(k) K173288
- Cleared FDA 510(k) K202275
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- CorPath GRX Drape, Control Console
- Generic name
- Cardiac mapping system workstation
- Model / Ref / Catalog
- 311
- Primary DI / UDI-DI
- 00816280023116
- FDA product code
- DXX
- GMDN term
- Cardiac mapping system workstation
- Device class
- Class II
- Regulation number
- 870.1290
- GUDID distribution status
- Not in Commercial Distribution
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