NEONATE PERCUSSOR— 510(k) K860510

Substantially Equivalent

Ballard Medical Products

FDA 510(k) clearance K860510 for NEONATE PERCUSSOR, Substantially Equivalent on 1986-02-20. Applicant: Ballard Medical Products.

Clearance details

Applicant: Ballard Medical Products
Product code: Code BYI
Advisory panel: Anesthesiology
Date received: 1986-02-11
Decision date: 1986-02-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Midvale, UT, US

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Adverse events under product code BYI

product code BYI

Death: 3
Total: 3

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.