GUIDANT RETRIEVER DEVICE


codes

Device Classification Name

catheter, percutaneous

510(k) Number K001694
Device Name GUIDANT RETRIEVER DEVICE
Original Applicant
GUIDANT CARDIAC AND VASCULAR SURGERY
1525 o’brien dr.
menlo park, 
CA 
94025

Original Contact bernice jurs
Regulation Number 870.1250
Classification Product Code
DQY  
Date Received 06/02/2000
Decision Date 05/15/2001
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

Type Traditional
Reviewed by Third Party No

Combination Product

No