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

HOMMED CENTRAL STATION

K Number: K020184 · Decision Apr 22, 2002
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
8
Review Days
94

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Basic Information

Device Name
HOMMED CENTRAL STATION
K Number
K020184
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1130
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hommed, LLC
Date Received
January 18, 2002
Decision Date
April 22, 2002
Product Code
DXN
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
DXN System, Measurement, Blood-Pressure, Non-Invasive

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Other Clearances by Hommed, LLC

K Number Device Name
K040799 HOMMED GENESIS PATIENT MONITOR SYSTEM WITH OPTIONS
K040651 HOMMED SENTRY IIIB-F PATIENT MONITOR SYSTEM
K040032 CENTRAL STATION, VERSION 3.3H
K014025 HOMMED SENTRY III PATIENT MONITOR SYSTEM WITH CARD READER
K003180 HOMMED OBSERVER, MODEL I
K004044 HOMMED SENTRY III PATIENT MONITOR SYSTEM
K993938 THE HOMMED SENTRY, MODEL 1 SENTRY