LIDCORAPID V2 MONITOR


Device Classification Name

computer, diagnostic, pre-programmed, single-function

510(k) Number K122247
Device Name LIDCORAPID V2 MONITOR
Applicant
LIDCO LTD.
16 orsman rd.
london, 

GB

n15qj

Applicant Contact gregory speller
Correspondent
LIDCO LTD.
16 orsman rd.
london, 

GB

n15qj

Correspodent Contact gregory speller
Regulation Number 870.1435
Classification Product Code
DXG  
Subsequent Product Code
GWQ  
Date Received 07/27/2012
Decision Date 03/20/2013
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

statement

statement

Type Traditional
Reviewed by Third Party No

Combination Product

No

Category: Uncategorized