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

ISTAND

K Number: K103266 · Decision Jun 3, 2011
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
86
Applicant Total
16
Review Days
211

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Basic Information

Device Name
ISTAND
K Number
K103266
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1570
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Optovue, Inc.
Date Received
November 4, 2010
Decision Date
June 3, 2011
Product Code
HLI
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
HLI Ophthalmoscope, Ac-Powered

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K130656 IFUSION
K121739 IVUE WITH NORMATIVE DATABASE
K122572 ICAM FUNDUS CAMERA
K120238 RTVUE XR OCT
K111505 RTVUE CAM WITH CORNEAL POWER UPGRADE
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