QUINTON Q-CATH, MODEL 000460


Device Classification Name

computer, diagnostic, programmable

510(k) Number K021906
Device Name QUINTON Q-CATH, MODEL 000460
Original Applicant
QUINTON, INC.
3303 monte villa pkwy.
bothell, 
WA 
98021 -8906

Original Contact karen browne
Regulation Number 870.1425
Classification Product Code
DQK  
Date Received 06/10/2002
Decision Date 09/04/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

summary

summary

Type Abbreviated
Reviewed by Third Party No

Combination Product

No