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

V-TRACE ECG BACKPAD

K Number: K761301 · Decision Jan 5, 1977
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
11
Review Days
14

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Basic Information

Device Name
V-TRACE ECG BACKPAD
K Number
K761301
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Ndm Corp.
Date Received
December 22, 1976
Decision Date
January 5, 1977
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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K810920 NDM DIATEMP INFANT ELECTROSURG. DISP. P.
K801158 NDM DIATEMP ELECTROSURGICAL DIS. PAD
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K772354 I.V. CATHETER
K772160 ELECTROSURGICAL GROUNDING PAD
K760312 ELECTRODE, PNS
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