FDA 510(k)

SOFT PLUG延长持续时间180锥形管道塞

K号: K213988 · 2022-06-03

决定日期2022-06-03

产品代码LZU

决定实质等同

器械摘要

SOFT PLUG Extended Duration 180 Tapered Canalicular Plug is the device name listed in this FDA 510(k) record. The listed applicant is Oasis Medical, Inc.. It received FDA 510(k) clearance on 2022-06-03 under 510(k) number K213988. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.

常见问题

What is the SOFT PLUG Extended Duration 180 Tapered Canalicular Plug?

SOFT PLUG Extended Duration 180 Tapered Canalicular Plug is a medical device that received FDA 510(k) clearance on 2022-06-03. The listed applicant is Oasis Medical, Inc.. The 510(k) number is K213988.

When did SOFT PLUG Extended Duration 180 Tapered Canalicular Plug receive FDA 510(k) clearance?

SOFT PLUG Extended Duration 180 Tapered Canalicular Plug received FDA 510(k) clearance on 2022-06-03, under 510(k) number K213988.

Who is the listed applicant for SOFT PLUG Extended Duration 180 Tapered Canalicular Plug?

The FDA 510(k) record lists Oasis Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOFT PLUG Extended Duration 180 Tapered Canalicular Plug?

The FDA product code for SOFT PLUG Extended Duration 180 Tapered Canalicular Plug is LZU.

列明Oasis Medical, Inc.为申报人的其他记录

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。

K162361软性延长持续时间180通道泪点塞

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。