Check-Flo G15650
Check-Flo G15650 (050818) is a Class II device made by Cook Incorporated, cleared under FDA 510(k) K173105 on 22 Mar 2018 and listed in FDA GUDID since 5 Oct 2020 (UDI-DI 00827002156500), 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 | Number00827002156500 | Date5 Oct 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK173105 | Date22 Mar 2018 | StatusActive |
Official records
- AccessGUDID record 00827002156500
- FDA 510(k) database K173105
Across registries
- FDA 510(k) K173105 decided 22 Mar 2018 Active
- FDA GUDID UDI-DI 00827002156500 listed 5 Oct 2020 Listed
Timeline
- Cleared FDA 510(k) K173105
- Listed FDA GUDID 00827002156500
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Check-Flo
- Generic name
- Endoscope channel support kit
- Model / Ref / Catalog
- G15650, 050818
- Primary DI / UDI-DI
- 00827002156500
- 510(k) Number
- FDA product code
- ODC
- GMDN term
- Endoscope channel support kit
- Device class
- Class II
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
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