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

C3 PATIENT MONITOR

K Number: K030931 · Decision May 9, 2003
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
411
Applicant Total
32
Review Days
45

Basic Information

Device Name
C3 PATIENT MONITOR
K Number
K030931
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ANALOGIC CORP.
Date Received
March 25, 2003
Decision Date
May 9, 2003
Product Code
MHX
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

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K043025 SYNERAD OMNI, DIGITAL X-RAY SYSTEM, MODEL AN6250
K041434 C3 AND LIFEGARD ICG IMPEDANCE CARDIOGRAPHY MONITORS
K041376 C1 SERIES PATIENT MONITOR, MODELS 863051, 863052, 863053, 863054; OPTIONAL PRINTER FOR CI, MODEL M3925A
K040995 SYNERAD MULTI DIGITAL X-RAY SYSTEM, MODEL AN6150
K033345 AN5150 AND AN7150 DIGITAL RADIOLOGY SYSTEMS
K011304 OB-1 FETAL MONITOR
K002503 FETALGARD LITE
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