Identity
- Trade Name
- ACETAMINOPHEN L3K FDA UDI
- Generic Name
- Acetaminophen IVD, kit, spectrophotometry FDA UDI
- Model / Reference
- 506-10 FDA UDI
Identifiers
- Catalog Number
- 506-10 FDA UDI
- Primary DI / UDI-DI
- 00628063400027 FDA UDI
- 510(k) Number
- K081938 FDA UDI
- FDA Product Code
- LDP FDA UDI
- GMDN Term
- Acetaminophen IVD, kit, spectrophotometry FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.3030 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Acetaminophen L3k by Sekisui Diagnostics, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K081938 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
- Sekisui Diagnostics, LLC
Sources (1)
- FDA UDI e1fe5301-b1c7-47a9-b6be-406142b79ab3 35 fields · synced Jun 9, 2026