STRYKER L3 HYDROLERT


Device Classification Name

monitor, electric for gravity flow infusion systems

510(k) Number K022248
Device Name STRYKER L3 HYDROLERT
Original Applicant
Stryker Endoscopy
5900 optical ct.
san jose, 
CA 
95138

Original Contact michael hilldoerfer
Regulation Number 880.2420
Classification Product Code
FLN  
Date Received 07/12/2002
Decision Date 08/06/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General Hospital

510k Review Panel

General & Plastic Surgery

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No