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

AMBULATORY BLOOD PRESSURE (ABP) 92506 REPORT MANAGEMENT SYSTEM (RMS), MODEL 92506

K Number: K031479 · Decision Jun 6, 2003
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
58
Review Days
29

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Basic Information

Device Name
AMBULATORY BLOOD PRESSURE (ABP) 92506 REPORT MANAGEMENT SYSTEM (RMS), MODEL 92506
K Number
K031479
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1130
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Datex-Ohmeda, Inc.
Date Received
May 8, 2003
Decision Date
June 6, 2003
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 Datex-Ohmeda, Inc.

K Number Device Name
K251663 Giraffe OmniBed Carestation (CS1); Giraffe Incubator Carestation (CS1)
K213867 Carestation 750/750c
K210384 CARESCAPE R860
K172702 Tec 820, Tec 850
K172045 Aestiva 7900, Aestiva MRI, Aestiva 7100, Aestiva 7100 Compact, Aespire 100, Aespire 7100, Aespire 7900, Aespire View, Avance, Avance CS2, Aisys, Aisys CS2
K170872 Aisys CS2
K151570 Carestation 620/650/650C
K142679 CARESCAPE R860
K143530 Aespire View
K140575 ENGSTROM CARESTATION, ENGSTROM PRO
Search all 58 clearances from Datex-Ohmeda, Inc. →