FDA 510(k)

緊咬緩解口器 PRO RX，緊咬緩解口器

K 號：K222845 · 2023-11-28

決定日期2023-11-28

產品代碼MQC

決定相當於

器材摘要

Clench Relief Mouth Piece PRO RX, Clench Relief Mouth Piece is the device name listed in this FDA 510(k) record. The listed applicant is Frey Oral Technologies, LLC. It received FDA 510(k) clearance on 2023-11-28 under 510(k) number K222845. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.

常見問題

What is the Clench Relief Mouth Piece PRO RX, Clench Relief Mouth Piece?

Clench Relief Mouth Piece PRO RX, Clench Relief Mouth Piece is a medical device that received FDA 510(k) clearance on 2023-11-28. The listed applicant is Frey Oral Technologies, LLC. The 510(k) number is K222845.

When did Clench Relief Mouth Piece PRO RX, Clench Relief Mouth Piece receive FDA 510(k) clearance?

Clench Relief Mouth Piece PRO RX, Clench Relief Mouth Piece received FDA 510(k) clearance on 2023-11-28, under 510(k) number K222845.

Who is the listed applicant for Clench Relief Mouth Piece PRO RX, Clench Relief Mouth Piece?

The FDA 510(k) record lists Frey Oral Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Clench Relief Mouth Piece PRO RX, Clench Relief Mouth Piece?

The FDA product code for Clench Relief Mouth Piece PRO RX, Clench Relief Mouth Piece is MQC.

相關器械（代碼：MQC）

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官方來源

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器材摘要

常見問題

相關臨床試驗

相關器械（代碼：MQC）

官方來源