Ear Pressure Relief Device(Model:ER813B)— 510(k) K230502

Name: FDA 510(k) clearance K230502
Creator: U.S. Food and Drug Administration
Published: 2023-06-09

Substantially Equivalent

Ningbo Albert Novosino Co., Ltd.

FDA 510(k) clearance K230502 for Ear Pressure Relief Device(Model:ER813B), Substantially Equivalent on 2023-06-09. Applicant: Ningbo Albert Novosino Co., Ltd.. Device class: Unclassified.

Clearance details

Applicant: Ningbo Albert Novosino Co., Ltd.
Product code: Code MJV
Device class: Unclassified
Advisory panel: Unknown
Date received: 2023-02-24
Decision date: 2023-06-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Yuyao, CN

Download summary PDF View on FDA.gov ↗

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