FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SEPRAGEL SINUS

K Number: K012532 · Decision Oct 30, 2001
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
45
Applicant Total
27
Review Days
85

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Basic Information

Device Name
SEPRAGEL SINUS
K Number
K012532
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.4780
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Genzyme Corp.
Date Received
August 6, 2001
Decision Date
October 30, 2001
Product Code
LYA
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
LYA Splint, Intranasal Septal

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