JTL-250-01
K号: K182732 · 2019-11-18
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决定日期2019-11-18
产品代码MUU
咨询委员会SU
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决定实质等同
器械摘要
JTL-250-01 is the device name listed in this FDA 510(k) record. The listed applicant is Jointechlabs, Inc.. It received FDA 510(k) clearance on 2019-11-18 under 510(k) number K182732. The device is classified under product code MUU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the JTL-250-01?
JTL-250-01 is a medical device that received FDA 510(k) clearance on 2019-11-18. The listed applicant is Jointechlabs, Inc.. The 510(k) number is K182732.
When did JTL-250-01 receive FDA 510(k) clearance?
JTL-250-01 received FDA 510(k) clearance on 2019-11-18, under 510(k) number K182732.
Who is the listed applicant for JTL-250-01?
The FDA 510(k) record lists Jointechlabs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JTL-250-01?
The FDA product code for JTL-250-01 is MUU.
相关器械（代码：MUU）
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