Oclet TDS 1000
K号: K212049 · 2022-03-08
广告
器械摘要
Oclet TDS 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Tendonova Corporation. It received FDA 510(k) clearance on 2022-03-08 under 510(k) number K212049. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.
常见问题
What is the Oclet TDS 1000?
Oclet TDS 1000 is a medical device that received FDA 510(k) clearance on 2022-03-08. The listed applicant is Tendonova Corporation. The 510(k) number is K212049.
When did Oclet TDS 1000 receive FDA 510(k) clearance?
Oclet TDS 1000 received FDA 510(k) clearance on 2022-03-08, under 510(k) number K212049.
Who is the listed applicant for Oclet TDS 1000?
The FDA 510(k) record lists Tendonova Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Oclet TDS 1000?
The FDA product code for Oclet TDS 1000 is LFL.
相关临床试验
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
相关器械（代码：LFL）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
K261448neXus 超声手术吸引器系统Misonix, LLCK251162CUSA® Clarity超声手术吸引器系统Integra LifeSciences CorporationK242894SanAgile® 超声手术高级便携式控制器 (SA10)；SanAgile® 超声手术高级解剖器 (SASD14)；SanAgile® 超声手术高级解剖器 (SASD23)；SanAgile® 超声手术高级解剖器 (SASD36)；SanAgile® 超声手术高级解剖器 (SASD45)Shanghai Saints Sages Surgical Co., Ltd.K243930Sonopet iQ 超声波吸引器系统 (5500-050-000)Stryker InstrumentsK241700Tenex 2代系统Trice Medical, Inc.K240493CUSA® Clarity超声手术吸引器系统Integra LifeSciences Corporation
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。
广告