FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇰 Denmark

LiNA OperaScope with HDMI cable and on-board LCD-single unit, LiNA OperaScope with HDMI cable and on-board LCD-6 units, LiNA OperaScope Recording Module

K Number: K171113 · Decision Jan 4, 2018
Classifications
1
FEI Numbers
135
Registration Numbers
135
Same Product Code
170
Applicant Total
16
Review Days
265

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Basic Information

Device Name
LiNA OperaScope with HDMI cable and on-board LCD-single unit, LiNA OperaScope with HDMI cable and on-board LCD-6 units, LiNA OperaScope Recording Module
K Number
K171113
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1690
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Lina Medical Aps
Date Received
April 14, 2017
Decision Date
January 4, 2018
Product Code
HIH
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HIH Hysteroscope (And Accessories)

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Other Clearances by Lina Medical Aps

K Number Device Name
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K221085 LiNA OperaScope Needle
K193007 LiNA OperaScope with HDMI cable and on-board LCD - 6 units, LiNA OperaScope Recording Module
K182224 SafeAir Smoke Evacuator compact
K182354 SafeAir Telescopic Smoke Pencil
K143145 SafeAir Smoke Pencil
K142757 LiNA PowerBlade Plus HC
K142538 LiNA SafeAir Smoke Pencil
K132135 LINA GOLD LOOP HC
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