FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

MEDTRONIC 6304, 6305,6306,6506 & 6506W. TEMP.PACIN

K Number: K844959 · Decision Jan 10, 1985
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
486
Applicant Total
468
Review Days
20

Basic Information

Device Name
MEDTRONIC 6304, 6305,6306,6506 & 6506W. TEMP.PACIN
K Number
K844959
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
MEDTRONIC VASCULAR
Date Received
December 21, 1984
Decision Date
January 10, 1985
Product Code
DTB
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
DTB Permanent Pacemaker Electrode

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