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

PeriView FLEX

K Number: K171232 · Decision Sep 21, 2017
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
27
Applicant Total
8
Review Days
147

Basic Information

Device Name
PeriView FLEX
K Number
K171232
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4680
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Olympus Surgical Technologies America
Date Received
April 27, 2017
Decision Date
September 21, 2017
Product Code
KTI
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
KTI Bronchoscope Accessory

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