Sola Commido Loupe

FDA 510(k) K760770 · Codman & Shurtleff, Inc.

Substantially Equivalent

510(k) numberK760770

Submission

Device name
Sola Commido Loupe
Applicant
Codman & Shurtleff, Inc.
Mchenry, IL, US
Received
October 4, 1976
Decision date
October 15, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

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

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K131959Heine Mini 3000(R) OphthalmoscopeHLJ · Abbreviated Heine Optotechnik GmbH & Co. KG03/07/2014SE
K131961Heine Beta 200(R) OphthalmoscopeHLJ · Abbreviated Heine Optotechnik GmbH & Co. KG12/04/2013SE
K131719Ophthalmoscopes Diagnostic Instrument KitsHLJ · Traditional Medical Devices (Pvt) , Ltd.10/30/2013SE
K123587Heine Mini 3000 LED OphthalmoscopeHLJ · Abbreviated Heine Optotechnik GmbH & Co. KG03/22/2013SE
K093495Otoscope and Ophthalmoscope Diagnostic Instrument KitsHLJ · Traditional American Diagnostic Corp.11/19/2010SE
K070270Piccolight E50,PICCOLIGHT E56,EUROLIGHT E10, Eurolight E30, and Eurolight E36HLJ · Traditional Kirchner & Wilhelm GmbH + Co.Kg11/05/2007SE
K05259966 Vision Tech Ophthalmoscope, Models YZ6E, YZ6F, YZ6G, YZ11, YZ11C, YZ11D, YZ25AHLJ · Traditional Suzhou 66 Vision Tech Co., Ltd.11/07/2006SE
K061278Optyse OphthalmoscopeHLJ · Abbreviated Ophthalmos , Ltd.05/16/2006SE

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Questions and answers

When was Sola Commido Loupe cleared by the FDA?

Sola Commido Loupe (K760770) received a 510(k) decision of Substantially Equivalent on October 15, 1976, 11 days after the submission was received.

What is the product code of K760770?

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