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

MEMORYTRACE ATM MODEL 4222

K Number: K941898 · Decision Jun 26, 1995
Classifications
1
FEI Numbers
80
Registration Numbers
80
Same Product Code
296
Applicant Total
2
Review Days
434

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Basic Information

Device Name
MEMORYTRACE ATM MODEL 4222
K Number
K941898
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2920
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Hi-Tronics Designs, Inc.
Date Received
April 18, 1994
Decision Date
June 26, 1995
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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Other Clearances by Hi-Tronics Designs, Inc.

K Number Device Name
K973863 MEMORYTRACE MODEL 4224 AMBULATORY ECG MONITOR