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

HILAL EMBOLIZATION MICROCOIL(TM)

K Number: K901337 · Decision Nov 13, 1990
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
184
Applicant Total
190
Review Days
236

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Basic Information

Device Name
HILAL EMBOLIZATION MICROCOIL(TM)
K Number
K901337
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5950
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Cook, Inc.
Date Received
March 22, 1990
Decision Date
November 13, 1990
Product Code
HCG
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
HCG Device, Neurovascular Embolization

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