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FDA 510(k)

Sunkingdom Slit Lamp

K-Number: K182306 · 2018-11-22

ApplicantChongqing Sunkingdom Medical Instrument Co., Ltd.
Decision Date2018-11-22
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

Sunkingdom Slit Lamp is the device name listed in this FDA 510(k) record. The listed applicant is Chongqing Sunkingdom Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2018-11-22 under 510(k) number K182306. The device is classified under product code HJO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Sunkingdom Slit Lamp?

Sunkingdom Slit Lamp is a medical device that received FDA 510(k) clearance on 2018-11-22. The listed applicant is Chongqing Sunkingdom Medical Instrument Co., Ltd.. The 510(k) number is K182306.

When did Sunkingdom Slit Lamp receive FDA 510(k) clearance?

Sunkingdom Slit Lamp received FDA 510(k) clearance on 2018-11-22, under 510(k) number K182306.

Who is the listed applicant for Sunkingdom Slit Lamp?

The FDA 510(k) record lists Chongqing Sunkingdom Medical Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sunkingdom Slit Lamp?

The FDA product code for Sunkingdom Slit Lamp is HJO.

Other records listing Chongqing Sunkingdom Medical Instrument Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K222787Sunkingdom Ophthalmic Ultrasound Examination Instrument SK-3000A, SK-3000B, SK-3000C, SK-2000AP, SK-2000A, SK-2000PK191314Sunkingdom Applanation Tonometer SK-R, SK-T, SK-Q

Related Devices (Code: HJO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253834VISUREF 600Carl Zeiss Vision GmbHK231760HP-OCT (HP-OCT)Cylite Pty. , Ltd.K222372Kowa SL-19Kowa Company , Ltd.K193188MiiS Horus Eye Anterior CameraMedimaging Integrated Solution, Inc (Miis)K173771IOLMaster 700Carl Zeiss Meditec, AGK171877SLM-1ER, SLM-2ER, SLM-3ERChongqing Kanghua Ruiming S&T Co., Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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