Identity
- Trade Name
- AccuBoost FDA UDI
- Generic Name
- General-purpose brachytherapy system applicator, manual FDA UDI
- Device Name
- Planmed - DV Low Profile Magnification Stand FDA UDI
- Model / Reference
- 450125-02 FDA UDI
- Description
- Planmed - DV Low Profile Magnification Stand FDA UDI
Identifiers
- Catalog Number
- PM-PA-MSLP FDA UDI
- Primary DI / UDI-DI
- 00850306007599 FDA UDI
- 510(k) Number
- K863890 FDA UDI
- FDA Product Code
- KXH FDA UDI
- GMDN Term
- General-purpose brachytherapy system applicator, manual FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 892.1830 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: General-purpose brachytherapy system applicator, manual
AccuBoost by Advanced Radiation Therapy, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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 I | Pending data |
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Manufacturer
- Manufacturer
- Advanced Radiation Therapy, Llc
Sources (1)
- FDA UDI 96a6d7b9-c8c6-48d2-947b-8d558285860c 36 fields · synced Jun 1, 2026