Eargo 5 , Eargo 6— 510(k) K221698

Substantially Equivalent

Eargo, Inc.

FDA 510(k) clearance K221698 for Eargo 5 , Eargo 6, Substantially Equivalent on 2022-12-21. Applicant: Eargo, Inc.. Device class: 2.

Clearance details

Applicant
Eargo, Inc.
Product code
Code QUH
Device class
Class 2
Regulation
21 CFR 874.3325
Advisory panel
Ear, Nose, Throat
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
San Jose, CA, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code QUH

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Adverse events under product code QUH

product code QUH
Other
1
Total
1

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.