ProcedureKitCRF CRF-N1010-K
by Cambridge Interventional LLC
ProcedureKitCRF CRF-N1010-K is a Class II device made by Cambridge Interventional LLC, cleared under FDA 510(k) K192715 on 7 Jan 2020 and listed in FDA GUDID since 13 Jan 2026 (UDI-DI 00811746033845), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00811746033845 | Date13 Jan 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK192715 | Date7 Jan 2020 | StatusActive |
Official records
- AccessGUDID record 00811746033845
- FDA 510(k) database K192715
Across registries
- FDA 510(k) K192715 decided 7 Jan 2020 Active
- FDA GUDID UDI-DI 00811746033845 listed 13 Jan 2026 Listed
Timeline
- Cleared FDA 510(k) K192715
- Listed FDA GUDID 00811746033845
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- ProcedureKitCRF
- Generic name
- Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar
- Model / Ref / Catalog
- CRF-N1010-K
- Primary DI / UDI-DI
- 00811746033845
- 510(k) Number
- FDA product code
- GEI
- GMDN term
- Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code GEI (Electrosurgical, Cutting & Coagulation & Accessories).
- THUNDERBEAT 5 mm, 10 cm, Inline Grip TB-0510IC by Olympus Medical Systems Corporation
- Guenter Bissinger Medizintechnik GmbH 80100219 by Günter Bissinger Medizintechnik GmbH
- LTC VAD SYSTEM, MODELS #VAD.400 (ELECTROSURGICAL GENERATOR); PCS-900 AND PCC-900 (HAND PIECE INSTRUMENTS) by Live Tissue Connect, Inc.
- MPI ELECTROSURGICAL CAPACTIVE DISPER by Medical Plastics, Inc.
- Voyant® Electrosurgical Generator (EA030/Electrosurgical Generator) by APPLIED MEDICAL RESOURCES CORP.
- ARTHROCARE SYSTEM 2000 CONTROLLER, ARTHROCARE SYSTEM 2000 CABLE, ARTHROCARE SYSTEM 2000 FOOTSWITCH, PLASMA SCALPEL GS, C by ArthroCare Corporation
- SURGICAL CUTTER by Promex, Inc.
- HOOK ELECTRODE, NEEDLE ELECTRODE, COAGULATION BUTTON ELECTRODE by RICHARD WOLF MEDICAL INSTRUMENTS CORP.
- RESECT MEDICAL INLINE BI-POLAR RF LINEAR COAGULATION DEVICE by Resect Medical, Inc.
- SKINTACT COOL CONTACT ELECTROSURGICAL GROUNDING PLATE WITH NH 04 GEL by Leonhard Lang Co.