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

ELECTRODE/EXTENSION CABLES, MODELS ATAR

K Number: K070926 · Decision Jun 7, 2007
Classifications
1
FEI Numbers
212
Registration Numbers
212
Same Product Code
5
Applicant Total
49
Review Days
65

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Basic Information

Device Name
ELECTRODE/EXTENSION CABLES, MODELS ATAR
K Number
K070926
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
890.1175
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Oscor, Inc.
Date Received
April 3, 2007
Decision Date
June 7, 2007
Product Code
IKD
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IKD Cable, Electrode

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K130843 SAFESEPT NEEDLE FREE TRANSSEPTAL TROCAR GUIDEWIRE
K130104 GUIDEWIRE, PURSUER SERIES
K122960 STEERABLE GUIDING SHEATH, MODEL ADELANTE DESTINO
K122958 DELIVERY SHEATH, MODEL ADELANTE BREEZEWAY
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