LOTUS Series 4 Enhanced Shears, LOTUS Series 5
K号: K221102 · 2022-12-15
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器械摘要
LOTUS Series 4 Enhanced Shears, LOTUS Series 5 is the device name listed in this FDA 510(k) record. The listed applicant is Sra Developments, Ltd.. It received FDA 510(k) clearance on 2022-12-15 under 510(k) number K221102. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.
常见问题
What is the LOTUS Series 4 Enhanced Shears, LOTUS Series 5?
LOTUS Series 4 Enhanced Shears, LOTUS Series 5 is a medical device that received FDA 510(k) clearance on 2022-12-15. The listed applicant is Sra Developments, Ltd.. The 510(k) number is K221102.
When did LOTUS Series 4 Enhanced Shears, LOTUS Series 5 receive FDA 510(k) clearance?
LOTUS Series 4 Enhanced Shears, LOTUS Series 5 received FDA 510(k) clearance on 2022-12-15, under 510(k) number K221102.
Who is the listed applicant for LOTUS Series 4 Enhanced Shears, LOTUS Series 5?
The FDA 510(k) record lists Sra Developments, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LOTUS Series 4 Enhanced Shears, LOTUS Series 5?
The FDA product code for LOTUS Series 4 Enhanced Shears, LOTUS Series 5 is LFL.
相关临床试验
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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。
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官方来源
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