FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

STAR 55

K Number: K080173 · Decision Feb 8, 2008
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
301
Applicant Total
18
Review Days
15

Basic Information

Device Name
STAR 55
K Number
K080173
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
LARSEN & TOUBRO LIMITED
Date Received
January 24, 2008
Decision Date
February 8, 2008
Product Code
MWI
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

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Other Clearances by LARSEN & TOUBRO LIMITED

K Number Device Name
K103686 STAR 50 N
K103763 STELLAR 300
K093017 STELLAR 300
K092153 SKYLINE 55, MODEL VER 1
K090443 PLANET 55, MODEL 100
K090172 STAR 55 MODEL 100
K082685 GALAXY 55
K081552 SKYLINE 55
K071472 PLANET 55
K061816 GALAXY
Search all 18 clearances from LARSEN & TOUBRO LIMITED →