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

3M RED DOT 2234 & 2266 RADIOLUCENT MONITORING ELECTRODES

K Number: K971444 · Decision Jun 11, 1997
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
12
Review Days
51

Basic Information

Device Name
3M RED DOT 2234 & 2266 RADIOLUCENT MONITORING ELECTRODES
K Number
K971444
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
3M MEDICAL PRODUCTS GROUP
Date Received
April 21, 1997
Decision Date
June 11, 1997
Product Code
DRX
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
DRX Electrode, Electrocardiograph

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