Identity
- Trade Name
- Fifty50 FDA UDI
- Generic Name
- Glucose IVD, reagent FDA UDI
- Device Name
- Fifty50 Blood Glucose Test Strip FDA UDI
- Model / Reference
- 163140 FDA UDI
- Description
- Fifty50 Blood Glucose Test Strip FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00892896000017 FDA UDI
- 510(k) Number
- K083468 FDA UDI
- FDA Product Code
- CGA FDA UDI
- GMDN Term
- Glucose IVD, reagent FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1345 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
Yes
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: Glucose IVD, reagent
Fifty50 by i-SENS, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Glucose IVD, reagent.
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Cleared under the same submission
K083468 also covers:
- GLUCOCARD® Shine XL Blood Glucose Monitoring System — ARKRAY USA, INC.
- GLUCOCARD® Shine XL Blood Glucose Monitoring System — ARKRAY USA, INC.
- CareSens N — i-SENS, Inc.
- CareSens N — i-SENS, Inc.
- CareSens N — i-SENS, Inc.
- CareSens N — i-SENS, Inc.
- CareSens N — i-SENS, Inc.
- CareSens N — i-SENS, Inc.
- CareSens N — i-SENS, Inc.
- CareSens N — i-SENS, Inc.
- CareSens N — i-SENS, Inc.
- CareSens N (MedPoint Diagnostics) — i-SENS, Inc.
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
- i-SENS, Inc.
Sources (1)
- FDA UDI ed837ba6-fcc4-45e7-bda3-1304d24d44dc 36 fields · synced Jun 1, 2026