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

OVS1 VIDEO SYSTEM

K Number: K123359 · Decision Dec 19, 2012
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
30
Applicant Total
1
Review Days
49

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Basic Information

Device Name
OVS1 VIDEO SYSTEM
K Number
K123359
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Olive Medical Corp.
Date Received
October 31, 2012
Decision Date
December 19, 2012
Product Code
FCW
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FCW Light Source, Fiberoptic, Routine

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