FDA PMA

人工乳房、充気式、内部、塩水式

PMA番号：P990074 · 2024-12-16

申請者Allergan

決定日2024-12-16

PMA番号P990074

製品コードFWM

デバイスクラスクラス3

診療科G

規制番号21 CFR 8

諮問委員会SU （以下のテキストは翻訳されていません。） Policy: medical-regulatory-v1

医療機器の概要

Prosthesis, breast, inflatable, internal, saline is the device name listed in this FDA 510(k) record. The listed applicant is Allergan. It received FDA 510(k) clearance on 2024-12-16. The device is classified under product code FWM. It was reviewed by the SU advisory panel.

よくある質問

What is the Prosthesis, breast, inflatable, internal, saline?

Prosthesis, breast, inflatable, internal, saline is a medical device that received FDA 510(k) clearance on 2024-12-16. The listed applicant is Allergan.

When did Prosthesis, breast, inflatable, internal, saline receive FDA 510(k) clearance?

The clearance date for Prosthesis, breast, inflatable, internal, saline can be found in the official FDA records.

Who is the listed applicant for Prosthesis, breast, inflatable, internal, saline?

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

What is the FDA product code for Prosthesis, breast, inflatable, internal, saline?

The FDA product code for Prosthesis, breast, inflatable, internal, saline is FWM.

公式ソース

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医療機器の概要

よくある質問

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