Identity
- Trade Name
- Accurett® FDA UDI
- Generic Name
- General cryosurgical system, cryogen gas, mechanical FDA UDI
- Model / Reference
- 8g cartridges for Accurett FDA UDI
Identifiers
- Catalog Number
- S-CO2-8G-BOX FDA UDI
- Primary DI / UDI-DI
- 15407008486003 FDA UDI
- 510(k) Number
- K161615 FDA UDI
- FDA Product Code
- GEH FDA UDI
- GMDN Term
- General cryosurgical system, cryogen gas, mechanical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4350 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
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
Yes
FDA UDI
Category: General cryosurgical system, cryogen gas, mechanical
Accurett® by H & O Equipments SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K161615 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
- H & O Equipments SA
Sources (1)
- FDA UDI 7c3f6afa-f615-4dc6-9d3f-819c74f67867 35 fields · synced Jun 8, 2026