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

ChitoZolve

K Number: K181696 · Decision Nov 30, 2018
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
45
Applicant Total
42
Review Days
156

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Basic Information

Device Name
ChitoZolve
K Number
K181696
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
Gyrus Acmi, Inc.
Date Received
June 27, 2018
Decision Date
November 30, 2018
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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