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

RTVUE CAM WITH CORNEAL POWER UPGRADE

K Number: K111505 · Decision Sep 8, 2011
Classifications
1
FEI Numbers
29
Registration Numbers
30
Same Product Code
65
Applicant Total
16
Review Days
100

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Basic Information

Device Name
RTVUE CAM WITH CORNEAL POWER UPGRADE
K Number
K111505
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
May 31, 2011
Decision Date
September 8, 2011
Product Code
OBO
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
OBO Tomography, Optical Coherence

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Other Clearances by Optovue, Inc.

K Number Device Name
K222166 SOLIX
K180660 Avanti
K163475 iVue
K153080 RTVue XR OCT Avanti with AngioVue Software
K133892 IVUE 500
K130656 IFUSION
K121739 IVUE WITH NORMATIVE DATABASE
K122572 ICAM FUNDUS CAMERA
K120238 RTVUE XR OCT
K103266 ISTAND
Search all 16 clearances from Optovue, Inc. →