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

FRANZ(TM) MOVEABLE STYLET MAP CATHETER, MODIFIED

K Number: K892207 · Decision Jun 12, 1989
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
182
Applicant Total
15
Review Days
70

Basic Information

Device Name
FRANZ(TM) MOVEABLE STYLET MAP CATHETER, MODIFIED
K Number
K892207
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1220
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
EP TECHNOLOGIES, INC.
Date Received
April 3, 1989
Decision Date
June 12, 1989
Product Code
DRF
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
DRF Catheter, Electrode Recording, Or Probe, Electrode Recording

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