MODEL 2500 PNEUMATIC PERCUSSOR— 510(k) K802399

Substantially Equivalent

Medical Equipment Development Co., Inc.

FDA 510(k) clearance K802399 for MODEL 2500 PNEUMATIC PERCUSSOR, Substantially Equivalent on 1980-10-23. Applicant: Medical Equipment Development Co., Inc..

Clearance details

Applicant: Medical Equipment Development Co., Inc.
Product code: Code BYI
Advisory panel: Anesthesiology
Date received: 1980-10-02
Decision date: 1980-10-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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.