Identity
- Trade Name
- AWARE FDA UDI
- Generic Name
- Clinical management support software FDA UDI
- Device Name
- Clinical decision support software indicated for use by licensed clinicians in a clinical setting integrated with Philips ICCA product. FDA UDI
- Model / Reference
- P1.0 FDA UDI
- Description
- Clinical decision support software indicated for use by licensed clinicians in a clinical setting integrated with Philips ICCA product. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850893007019 FDA UDI
- 510(k) Number
- K143372 FDA UDI
- FDA Product Code
- MWI FDA UDI
- GMDN Term
- Clinical management support software FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2300 FDA UDI
- Commercial Distribution
- 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Clinical management support software
Aware by Ambient Clinical Analytics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K143372 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Ambient Clinical Analytics
Sources (1)
- FDA UDI a76beb61-b224-4ef1-bf40-da6ea7ef8bc2 34 fields · synced May 30, 2026