FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

AMPLIFIER, PC-700

K Number: K780116 · Decision Feb 24, 1978
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
17
Applicant Total
38
Review Days
35

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Basic Information

Device Name
AMPLIFIER, PC-700
K Number
K780116
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
870.2390
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Burdick Corp.
Date Received
January 20, 1978
Decision Date
February 24, 1978
Product Code
DQC
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
DQC Phonocardiograph

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K900729 NEOSERV 824
K885085 ERGOMED 840/ERGOMED 840L
K892835 E350 ELECTROCARDIOGRAPH
K883440 E550 ELECTROCARDIOGRAPH
K873774 M300 MONITOR/CONTROLLER T500 TREADMILL
K870920 ELITE ELECTROCARDIOGRAPH
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