SLM-1ER, SLM-2ER, SLM-3ER
K-Number: K171877 · 2017-12-21
Decision Date2017-12-21
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
SLM-1ER, SLM-2ER, SLM-3ER is a medical device manufactured by Chongqing Kanghua Ruiming S&T Co., Ltd.. It received FDA 510(k) clearance on 2017-12-21 under approval 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. It is manufactured by Chongqing Kanghua Ruiming S&T Co., Ltd.. The 510(k) number is K171877.
When was SLM-1ER, SLM-2ER, SLM-3ER approved by the FDA?
SLM-1ER, SLM-2ER, SLM-3ER received FDA 510(k) clearance on 2017-12-21, under approval number K171877.
What company makes SLM-1ER, SLM-2ER, SLM-3ER?
SLM-1ER, SLM-2ER, SLM-3ER is manufactured by Chongqing Kanghua Ruiming S&T Co., Ltd..
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.
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Official Source
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