Identity
- Trade Name
- Athelas Home FDA UDI
- Generic Name
- Laboratory analyser cuvette IVD, single-use FDA UDI
- Model / Reference
- 850-00002-00 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 20860008385868 FDA UDI
- 510(k) Number
- K200828 FDA UDI
- FDA Product Code
- GKZ FDA UDI
- GMDN Term
- Laboratory analyser cuvette IVD, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.5220 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Laboratory analyser cuvette IVD, single-use
Athelas Home by Athelas — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K200828 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Athelas
Sources (1)
- FDA UDI 03ed84a8-eaff-4b70-af27-108ca346009c 33 fields · synced Jun 8, 2026