FDA 510(k)

Pac-Dent 牙托基树脂

K号: K210189 · 2021-07-28

决定日期2021-07-28

产品代码EBI

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决定实质等同

器械摘要

Pac-Dent Denture Base Resin is the device name listed in this FDA 510(k) record. The listed applicant is Pac-Dent, Inc.. It received FDA 510(k) clearance on 2021-07-28 under 510(k) number K210189. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Pac-Dent Denture Base Resin?

Pac-Dent Denture Base Resin is a medical device that received FDA 510(k) clearance on 2021-07-28. The listed applicant is Pac-Dent, Inc.. The 510(k) number is K210189.

When did Pac-Dent Denture Base Resin receive FDA 510(k) clearance?

Pac-Dent Denture Base Resin received FDA 510(k) clearance on 2021-07-28, under 510(k) number K210189.

Who is the listed applicant for Pac-Dent Denture Base Resin?

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

What is the FDA product code for Pac-Dent Denture Base Resin?

The FDA product code for Pac-Dent Denture Base Resin is EBI.

列明Pac-Dent, Inc.为申报人的其他记录

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