ANGIOTECH CVC


Device Classification Name

catheter,intravascular,therapeutic,short-term less than 30 days

510(k) Number K073520
Device Name ANGIOTECH CVC
Applicant
ANGIOTECH PHARMACEUTICALS, INC.
13921 park center road
suite 100
herndon, 
VA 
20171

Applicant Contact trudy d estridge
Correspondent
ANGIOTECH PHARMACEUTICALS, INC.
13921 park center road
suite 100
herndon, 
VA 
20171

Correspodent Contact trudy d estridge
Regulation Number 880.5200
Classification Product Code
FOZ  
Date Received 12/14/2007
Decision Date 04/11/2008
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General Hospital

510k Review Panel

General Hospital

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

Yes