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

COMPUTER

K Number: K844665 · Decision Feb 13, 1985
Classifications
1
FEI Numbers
63
Registration Numbers
63
Same Product Code
176
Applicant Total
38
Review Days
75

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Basic Information

Device Name
COMPUTER
K Number
K844665
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1435
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Burdick Corp.
Date Received
November 30, 1984
Decision Date
February 13, 1985
Product Code
DXG
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
DXG Computer, Diagnostic, Pre-Programmed, Single-Function

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Other Clearances by Burdick Corp.

K Number Device Name
K942565 ALTAIR-DISC RECORDER
K941351 BURDICK PRO2 OXIMETER
K904032 ELITE II ELECTROCARDIOGRAPH
K903565 E560 ELECTROCARDIOGRAPH
K900729 NEOSERV 824
K885085 ERGOMED 840/ERGOMED 840L
K892835 E350 ELECTROCARDIOGRAPH
K883440 E550 ELECTROCARDIOGRAPH
K873774 M300 MONITOR/CONTROLLER T500 TREADMILL
K870920 ELITE ELECTROCARDIOGRAPH
Search all 38 clearances from Burdick Corp. →