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FDA 510(k)

SLM-1ER, SLM-2ER, SLM-3ER

K-Number: K171877 · 2017-12-21

ApplicantChongqing Kanghua Ruiming S&T Co., Ltd.
Decision Date2017-12-21
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SLM-1ER, SLM-2ER, SLM-3ER is the device name listed in this FDA 510(k) record. The listed applicant is Chongqing Kanghua Ruiming S&T Co., Ltd.. It received FDA 510(k) clearance on 2017-12-21 under 510(k) number K171877. 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 SLM-1ER, SLM-2ER, SLM-3ER?

SLM-1ER, SLM-2ER, SLM-3ER is a medical device that received FDA 510(k) clearance on 2017-12-21. The listed applicant is Chongqing Kanghua Ruiming S&T Co., Ltd.. The 510(k) number is K171877.

When did SLM-1ER, SLM-2ER, SLM-3ER receive FDA 510(k) clearance?

SLM-1ER, SLM-2ER, SLM-3ER received FDA 510(k) clearance on 2017-12-21, under 510(k) number K171877.

Who is the listed applicant for SLM-1ER, SLM-2ER, SLM-3ER?

The FDA 510(k) record lists Chongqing Kanghua Ruiming S&T Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SLM-1ER, SLM-2ER, SLM-3ER?

The FDA product code for SLM-1ER, SLM-2ER, SLM-3ER is HJO.

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.

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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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