MLC Endothelial Cell Counter

FDA 510(k) K863970 · Mlc Technologies

Substantially Equivalent

510(k) numberK863970

Submission

Device name
MLC Endothelial Cell Counter
Applicant
Mlc Technologies
Ridgefield, CT, US
Received
October 14, 1986
Decision date
December 29, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HJO – Biomicroscope, Slit-Lamp, Ac-Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 886.1850
Specialty
Ophthalmic

Other 510(k)s with product code HJO

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K222372Kowa SL-19HJO · Traditional Kowa Company , Ltd.11/21/2022SE
K193188MiiS Horus Eye Anterior CameraHJO · Traditional Medimaging Integrated Solution, Inc (Miis)01/14/2020SE
K182306Sunkingdom Slit LampHJO · Traditional Chongqing Sunkingdom Medical Instrument Co., Ltd.11/22/2018SE
K173771IOLMaster 700HJO · Traditional Carl Zeiss Meditec, AG08/24/2018SE
K171877SLM-1ER, SLM-2ER, SLM-3ERHJO · Traditional Chongqing Kanghua Ruiming S&T Co., Ltd.12/21/2017SE
K170470Digital Eye Anterior CameraHJO · Traditional Medimaging Integrated Solution, Inc (Miis)10/06/2017SE
K162778Portable Slit Lamp MicroscopeHJO · Traditional Suzhou Kangjie Medical, Inc.07/21/2017SE
K162684SL 220HJO · Traditional Carl Zeiss Meditec, AG05/31/2017SE

Questions and answers

When was MLC Endothelial Cell Counter cleared by the FDA?

MLC Endothelial Cell Counter (K863970) received a 510(k) decision of Substantially Equivalent on December 29, 1986, 76 days after the submission was received.

What is the product code of K863970?

The FDA product code is HJO – Biomicroscope, Slit-Lamp, Ac-Powered, a Class II (moderate risk) device regulated under 21 CFR 886.1850.