Identity
- Trade Name
- QBC Diagnostics FDA UDI
- Generic Name
- Full blood count IVD, control FDA UDI
- Device Name
- QBC Hematology Controls FDA UDI
- Model / Reference
- 424304 FDA UDI
- Description
- QBC Hematology Controls FDA UDI
Identifiers
- Catalog Number
- 424304 FDA UDI
- Primary DI / UDI-DI
- 00858092006277 FDA UDI
- 510(k) Number
- K984099 FDA UDI
- FDA Product Code
- JPK FDA UDI
- GMDN Term
- Full blood count IVD, control FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.8625 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
No
FDA UDI
Category: Full blood count IVD, control
QBC Diagnostics by Drucker Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K984099 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
- Drucker Diagnostics
Sources (1)
- FDA UDI 688d5669-f45c-4e47-9314-8612a2a9422f 35 fields · synced Jun 8, 2026