NEURORECOVERY VENTRICULAR CATHETER & MAIN VALVE ASSEMBLY KIT


Device Classification Name

device, monitoring, intracranial pressure

510(k) Number K022638
Device Name NEURORECOVERY VENTRICULAR CATHETER & MAIN VALVE ASSEMBLY KIT
Original Applicant
NEURORECOVERY, INC.
49 plain st.
north attleboro, 
MA 
02760

Original Contact rosina robinson
Regulation Number 882.1620
Classification Product Code
GWM  
Date Received 08/08/2002
Decision Date 10/31/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Neurology

510k Review Panel

Neurology

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No