AUDIOMETER, RECORDING, AUTOMATIC— 510(k) K772169

Substantially Equivalent

B&K Instruments, Inc.

FDA 510(k) clearance K772169 for AUDIOMETER, RECORDING, AUTOMATIC, Substantially Equivalent on 1977-12-02. Applicant: B&K Instruments, Inc..

Clearance details

Applicant: B&K Instruments, Inc.
Product code: Code EWO
Advisory panel: Ear, Nose, Throat
Date received: 1977-11-18
Decision date: 1977-12-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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Adverse events under product code EWO

product code EWO

Other: 2
Total: 2

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.