FDA 510(k)

PANPAC 可弃真空刮匙

K号: K161106 · 2017-01-13

决定日期2017-01-13

产品代码HGH

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决定实质等同

器械摘要

PANPAC DISPOSABLE VACUUM CURETTES is the device name listed in this FDA 510(k) record. The listed applicant is Panpac Medical Corporation. It received FDA 510(k) clearance on 2017-01-13 under 510(k) number K161106. The device is classified under product code HGH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the PANPAC DISPOSABLE VACUUM CURETTES?

PANPAC DISPOSABLE VACUUM CURETTES is a medical device that received FDA 510(k) clearance on 2017-01-13. The listed applicant is Panpac Medical Corporation. The 510(k) number is K161106.

When did PANPAC DISPOSABLE VACUUM CURETTES receive FDA 510(k) clearance?

PANPAC DISPOSABLE VACUUM CURETTES received FDA 510(k) clearance on 2017-01-13, under 510(k) number K161106.

Who is the listed applicant for PANPAC DISPOSABLE VACUUM CURETTES?

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

What is the FDA product code for PANPAC DISPOSABLE VACUUM CURETTES?

The FDA product code for PANPAC DISPOSABLE VACUUM CURETTES is HGH.

列明Panpac Medical Corporation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。

K173351Panpac柔性托盘阴道托 K153422Panpac一次性阴道托植入器套装

官方来源

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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。