Amico DH-W35 Ophthalmoscope Series

FDA 510(k) K131939 · Amico Diagnostic Incorporated

Substantially Equivalent

510(k) numberK131939

Submission

Device name
Amico DH-W35 Ophthalmoscope Series
Applicant
Amico Diagnostic Incorporated
Apollo Beach, FL, US
Received
June 27, 2013
Decision date
March 26, 2014
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HLI – Ophthalmoscope, Ac-Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 886.1570
Specialty
Ophthalmic

Other 510(k)s with product code HLI

510(k)DeviceApplicantDecision
K153080RTVue XR OCT Avanti with AngioVue SoftwareHLI · Traditional Optovue, Inc.02/11/2016SE
K150722EnFocus 2300, EnFocus 4400HLI · Traditional Bioptigen, Inc.12/02/2015SE
K142953OCT-CameraHLI · Traditional Optomedical Technologies GmbH03/04/2015SE
K141638Propper Insight Binocular Indirect OphthalmosopeHLI · Abbreviated Propper Manufacturing Co., Inc.09/17/2014SE
K133758Centervue Macular Integrity AssessmentHLI · Traditional Centervue S.P.A.04/23/2014SE
K133892Ivue 500HLI · Traditional Optovue, Inc.03/19/2014SE
K123316Heine Omega 500HLI · Abbreviated Heine Optotechnik GmbH & Co. KG02/26/2013SE
K121739Ivue with Normative DatabaseHLI · Traditional Optovue, Inc.01/18/2013SE
K120057Envisu Spectral Domain Ophthalmic Imaging System (Sdois)HLI · Traditional Bioptigen, Inc.05/11/2012SE
K120238Rtvue XR OctHLI · Special Optovue, Inc.04/03/2012SE

Questions and answers

When was Amico DH-W35 Ophthalmoscope Series cleared by the FDA?

Amico DH-W35 Ophthalmoscope Series (K131939) received a 510(k) decision of Substantially Equivalent on March 26, 2014, 272 days after the submission was received.

What is the product code of K131939?

The FDA product code is HLI – Ophthalmoscope, Ac-Powered, a Class II (moderate risk) device regulated under 21 CFR 886.1570.