Phoenix Diagnostics 16-218
Phoenix Diagnostics 16-218 is a Class II device made by Phoenix Diagnostics, Inc., cleared under FDA 510(k) K013451 on 18 Dec 2001 and listed in FDA GUDID since 26 Apr 2017 (UDI-DI 00853366007288), active 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 | GUDID listing | Number00853366007288 | Date26 Apr 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK013451 | Date18 Dec 2001 | StatusActive |
Official records
- AccessGUDID record 00853366007288
- FDA 510(k) database K013451
Across registries
- FDA 510(k) K013451 decided 18 Dec 2001 Active
- FDA GUDID UDI-DI 00853366007288 listed 26 Apr 2017 Listed
Timeline
- Cleared FDA 510(k) K013451
- Listed FDA GUDID 00853366007288
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Phoenix Diagnostics
- Generic name
- Potassium (K+) IVD, calibrator
- Model / Ref / Catalog
- 16-218
- Primary DI / UDI-DI
- 00853366007288
- 510(k) Number
- FDA product code
- JIT
- GMDN term
- Potassium (K+) IVD, calibrator
- Device class
- Class II
- Regulation number
- 862.1150
- GUDID distribution status
- In Commercial Distribution
- Size
- Total Volume — 30 Milliliter
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