Medic Lux Diagnostic Sets

FDA 510(k) K832437 · Keeler Instruments, Inc.

Substantially Equivalent

510(k) numberK832437

Submission

Device name
Medic Lux Diagnostic Sets
Applicant
Keeler Instruments, Inc.
Mchenry, IL, US
Received
July 25, 1983
Decision date
August 16, 1983
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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K123587Heine Mini 3000 LED OphthalmoscopeHLJ · Abbreviated Heine Optotechnik GmbH & Co. KG03/22/2013SE
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K061278Optyse OphthalmoscopeHLJ · Abbreviated Ophthalmos , Ltd.05/16/2006SE

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K100500PSL Classic Slit LampHJO · Traditional 03/09/2010SE
K062412CryomaticHRN · Traditional 11/06/2006SE
K060822Vantage Indirect OphthalmoscopeHLI · Special 05/23/2006SE
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K992954Keeler Cryo Master & ProbesHRN · Traditional 12/21/1999SE
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Questions and answers

When was Medic Lux Diagnostic Sets cleared by the FDA?

Medic Lux Diagnostic Sets (K832437) received a 510(k) decision of Substantially Equivalent on August 16, 1983, 22 days after the submission was received.

What is the product code of K832437?

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