LCCS INSULATED SPINAL NEEDLE (RF CANNULA)


Device Classification Name

probe, radiofrequency lesion

510(k) Number K112231
Device Name LCCS INSULATED SPINAL NEEDLE (RF CANNULA)
Applicant
LCCS PRODUCTS LIMITED
05c fujai kangle building
nanshan district
shenzhen, guangdong, 

CN

518000

Applicant Contact field fu
Regulation Number 882.4725
Classification Product Code
GXI  
Date Received 08/04/2011
Decision Date 08/19/2011
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Neurology

510k Review Panel

Neurology

Type Traditional
Reviewed by Third Party Yes

Combination Product

No