Identity
- Trade Name
- OCCObaby FDA UDI
- Generic Name
- Infrared patient thermometer, skin FDA UDI
- Device Name
- The Non-contact Infrared Thermometer uses infrared sensor (thermopile) to detect the radiated infrared energy emitted by the object, solid, liquid or gas. The intensity of the emitted energy depends on the temperature of the object and the infrared sensor can recognize it to transfer to the proper electronic signal. The electronic signal can be processed in the subject device to convert to the temperature reading. Therefore, the subject device is able to measure the temperature of a person by the energy the person emits. FDA UDI
- Model / Reference
- OCCOscan FDA UDI
- Description
- The Non-contact Infrared Thermometer uses infrared sensor (thermopile) to detect the radiated infrared energy emitted by the object, solid, liquid or gas. The intensity of the emitted energy depends on the temperature of the object and the infrared sensor can recognize it to transfer to the proper electronic signal. The electronic signal can be processed in the subject device to convert to the temperature reading. Therefore, the subject device is able to measure the temperature of a person by the energy the person emits. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00863101000313 FDA UDI
- 510(k) Number
- K131243 FDA UDI
- FDA Product Code
- FLL FDA UDI
- GMDN Term
- Infrared patient thermometer, skin FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.2910 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
OCCObaby by Deocco Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K131243 also covers:
- Fever Thermometer — BETTER BASICS, INC.
- Fever therometer — BETTER BASICS, INC.
- Dagamma — DAGAMMA INC.
- Infrared Forehead Thermometer — Dynarex Corp.
- ProHT — Inland Products, Inc.
- MedOne — MEDONE LLC
- iProvèn — Masena Invest B.V.
- iProvèn — Masena Invest B.V.
- iProvèn — Masena Invest B.V.
- iProvèn — Masena Invest B.V.
- iProvèn — Masena Invest B.V.
- iProvèn — Masena Invest B.V.
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
- Deocco Llc
Sources (1)
- FDA UDI a0b5a881-3669-4b88-9f23-7efa009bea47 35 fields · synced Jun 1, 2026