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

CMOS Video-Rhino-Laryngoscope System

K Number: K182186 · Decision Mar 22, 2019
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
161
Applicant Total
334
Review Days
221

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Basic Information

Device Name
CMOS Video-Rhino-Laryngoscope System
K Number
K182186
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4760
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
KARL STORZ Endoscopy-America, Inc.
Date Received
August 13, 2018
Decision Date
March 22, 2019
Product Code
EOB
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
EOB Nasopharyngoscope (Flexible Or Rigid)

Similar 510(k) Clearances

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Other Clearances by KARL STORZ Endoscopy-America, Inc.

K Number Device Name
K252624 KARL STORZ Laryngoscopes and Accessories
K223923 HOPKINS Telescopes
K202957 Flexible Video Cysto-Urethroscope (C-view)
K200318 UNIDRIVE S II ENT, DrillCut-X II-35 Shaver Handpiece, DrillCut-X II-35 N Shaver Handpiece
K201135 Image1 S CCU, Image1 S 4U Camera Head
K200740 HD Video Rhino Laryngoscope
K191357 Flexible HD Cysto-Urethroscope System
K182723 Flexible HD Cysto-Urethroscope System
K183264 Flex-THOR scope
K182696 Telepack X LED
Search all 334 clearances from KARL STORZ Endoscopy-America, Inc. →