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

NORAPAD PLAIN; NORAPAD TA

K Number: K014268 · Decision Mar 27, 2002
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
23
Applicant Total
1
Review Days
90

Basic Information

Device Name
NORAPAD PLAIN; NORAPAD TA
K Number
K014268
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4700
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
PERLEI MEDICAL, INC.
Date Received
December 27, 2001
Decision Date
March 27, 2002
Product Code
HBA
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
HBA Neurosurgical Paddie

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