Identity
- Trade Name
- Temp probe FDA UDI
- Generic Name
- Noninvasive vascular ultrasound system, line-powered FDA UDI
- Device Name
- Foot temperature probe for Smartdop Dopplers. FDA UDI
- Model / Reference
- TP-02 FDA UDI
- Description
- Foot temperature probe for Smartdop Dopplers. FDA UDI
Identifiers
- Catalog Number
- TP-02 FDA UDI
- Primary DI / UDI-DI
- 00894912002906 FDA UDI
- 510(k) Number
- K131623 FDA UDI
- FDA Product Code
- JOP FDA UDI
- GMDN Term
- Noninvasive vascular ultrasound system, line-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2880 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
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Temp probe by Koven Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K131623 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
- Koven Technology, Inc.
Sources (1)
- FDA UDI 00dd5c21-7d72-4eee-8cf1-3091942a0ae9 37 fields · synced Jun 9, 2026