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510(k) K771572

Device
PATIENT MONITORS MODELS 78701A/78702A
Applicant
Hewlett-Packard Co.
510(k) number
K771572
Product code
DRR
Decision
Substantially Equivalent (SESE)
Decision date
1977-08-30
Date received
1977-08-15
Regulation
870.2050
Classification name
Amplifier And Signal Conditioner, Biopotential
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Third party reviewed
N

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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510(k), Device, Applicant table
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K802282ESOPHAGEAL ECG PREAMPLIFIER & SIGNAL CONConsolidated Medical Equipment, Inc.1980-10-10
K792283ESOPHAGEAL ECG PREAMPLIFIER & SIGNAL CONArzbaecher & Co.1979-11-21