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

CRITIKON CENTRAL STATIN MONITOR

K Number: K933404 · Decision Feb 9, 1994
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
51
Review Days
212

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Basic Information

Device Name
CRITIKON CENTRAL STATIN MONITOR
K Number
K933404
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Critikon Company, LLC
Date Received
July 12, 1993
Decision Date
February 9, 1994
Product Code
DPS
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
DPS Electrocardiograph

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K982342 DINAMAP MPS SELECT PORTABLE MONITOR
K943709 DINAMAP PLUS VITAL SIGNS MONOITOR
K942700 DINAMAP VITAL SIGNS MONITOR MODELS 9300 AND 9320/9340
K933050 CHANGES TO PROTECTIV(TM) & JELCO(TM) WINGED CATH
K915697 CRITIKON VITAL SIGNS MODULE
K921295 INTRAVENOUS CATHETERS MODIFICATIONS
K912188 DINAMAP PLUS PHYSIOLOGICAL MONITOR MODEL 8700
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