Appasamy Slit Lamp, A1A-11 and A1A-12 Series

FDA 510(k) K082031 · Appasamy Associates

Substantially Equivalent

510(k) numberK082031

Submission

Device name
Appasamy Slit Lamp, A1A-11 and A1A-12 Series
Applicant
Appasamy Associates
Arumbakkam, Chennai, IN
Received
July 17, 2008
Decision date
July 31, 2008
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

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

510(k)DeviceApplicantDecision
K253834Visuref 600HJO · Traditional Carl Zeiss Vision GmbH03/18/2026SE
K231760Hp-Oct (Hp-Oct)HJO · Traditional Cylite Pty. , Ltd.03/08/2024SE
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

More from Carl Zeiss Meditec, AG

510(k)DeviceDecision
K110205AAIO-7, Aaio WirlessHLI · Traditional 02/09/2011SE

Questions and answers

When was Appasamy Slit Lamp, A1A-11 and A1A-12 Series cleared by the FDA?

Appasamy Slit Lamp, A1A-11 and A1A-12 Series (K082031) received a 510(k) decision of Substantially Equivalent on July 31, 2008, 14 days after the submission was received.

What is the product code of K082031?

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