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ElectrodeCRF CRF-U1015T

by Cambridge Interventional LLC

ElectrodeCRF CRF-U1015T 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 3 Feb 2023 (UDI-DI 00811746033067), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K192715

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00811746033067 UDI-DI Date3 Feb 2023ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK192715 Date7 Jan 2020DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K192715 decided 7 Jan 2020 Active
  • FDA GUDID UDI-DI 00811746033067 listed 3 Feb 2023 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K192715
  2. Listed FDA GUDID 00811746033067

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
ElectrodeCRF
Generic name
Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar
Model / Ref / Catalog
CRF-U1015T
Primary DI / UDI-DI
00811746033067
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

Related devices

Category: Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar

Cleared under the same submission (K192715)

and 8 more cleared under K192715

Similar devices

Other devices filed under FDA product code GEI (Electrosurgical, Cutting & Coagulation & Accessories).

Other devices from Cambridge Interventional LLC

See all devices from Cambridge Interventional LLC →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)