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

ACCELERATED TRANSMISSION PROTOCOL

K Number: K955060 · Decision Apr 8, 1996
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
292
Applicant Total
32
Review Days
158

Basic Information

Device Name
ACCELERATED TRANSMISSION PROTOCOL
K Number
K955060
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2920
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
INSTROMEDIX, INC.
Date Received
November 2, 1995
Decision Date
April 8, 1996
Product Code
DXH
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
DXH Transmitters And Receivers, Electrocardiograph, Telephone

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