Hemoglobin AD Control HC-120
Hemoglobin AD Control HC-120 is a Class II device made by Analytical Control Systems, cleared under FDA 510(k) K802569 on 12 Nov 1980 and listed in FDA GUDID since 31 Jan 2019 (UDI-DI 00817869020229), 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 | Number00817869020229 | Date31 Jan 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK802569 | Date12 Nov 1980 | StatusActive |
Official records
- AccessGUDID record 00817869020229
- FDA 510(k) database K802569
Across registries
- FDA 510(k) K802569 decided 12 Nov 1980 Active
- FDA GUDID UDI-DI 00817869020229 listed 31 Jan 2019 Listed
Timeline
- Cleared FDA 510(k) K802569
- Listed FDA GUDID 00817869020229
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Hemoglobin AD Control
- Generic name
- Inherited haemoglobinopathy IVD, control
- Model / Ref / Catalog
- HC-120
- Primary DI / UDI-DI
- 00817869020229
- 510(k) Number
- FDA product code
- KHG
- GMDN term
- Inherited haemoglobinopathy IVD, control
- Device class
- Class II
- Regulation number
- 864.7500
- GUDID distribution status
- In Commercial Distribution
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