FDA 510(k)

Laon 正骨科

K号: K250198 · 2025-04-23

决定日期2025-04-23

产品代码PNN

咨询委员会DE

决定Substantially Equivalent

器械摘要

Laon Ortho is the device name listed in this FDA 510(k) record. The listed applicant is Laon Medi, Inc.. It received FDA 510(k) clearance on 2025-04-23 under 510(k) number K250198. The device is classified under product code PNN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Laon Ortho?

Laon Ortho is a medical device that received FDA 510(k) clearance on 2025-04-23. The listed applicant is Laon Medi, Inc.. The 510(k) number is K250198.

When did Laon Ortho receive FDA 510(k) clearance?

Laon Ortho received FDA 510(k) clearance on 2025-04-23, under 510(k) number K250198.

Who is the listed applicant for Laon Ortho?

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

What is the FDA product code for Laon Ortho?

The FDA product code for Laon Ortho is PNN.

列明Laon Medi, Inc.为申报人的其他记录

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