Endoeye Flex Deflectable Videoscope Olympus LTF-S190-5
K号: K201832 · 2021-09-17
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决定日期2021-09-17
产品代码HET
咨询委员会OB
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决定实质等同
器械摘要
Endoeye Flex Deflectable Videoscope Olympus LTF-S190-5 is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Medical Systems Corp.. It received FDA 510(k) clearance on 2021-09-17 under 510(k) number K201832. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Endoeye Flex Deflectable Videoscope Olympus LTF-S190-5?
Endoeye Flex Deflectable Videoscope Olympus LTF-S190-5 is a medical device that received FDA 510(k) clearance on 2021-09-17. The listed applicant is Olympus Medical Systems Corp.. The 510(k) number is K201832.
When did Endoeye Flex Deflectable Videoscope Olympus LTF-S190-5 receive FDA 510(k) clearance?
Endoeye Flex Deflectable Videoscope Olympus LTF-S190-5 received FDA 510(k) clearance on 2021-09-17, under 510(k) number K201832.
Who is the listed applicant for Endoeye Flex Deflectable Videoscope Olympus LTF-S190-5?
FDA 510(k)记录中列出Olympus Medical Systems Corp.为申请人。这本身并不足以确立该设备制造商的身份。
What is the FDA product code for Endoeye Flex Deflectable Videoscope Olympus LTF-S190-5?
The FDA product code for Endoeye Flex Deflectable Videoscope Olympus LTF-S190-5 is HET.
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列明Olympus Medical Systems Corp.为申报人的其他记录
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官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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