ARGYLE PEOCUSSOR SYSTEM— 510(k) K771876

Name: FDA 510(k) clearance K771876
Creator: U.S. Food and Drug Administration
Published: 1977-10-28

Substantially Equivalent

Sherwood Medical Industries

FDA 510(k) clearance K771876 for ARGYLE PEOCUSSOR SYSTEM, Substantially Equivalent on 1977-10-28. Applicant: Sherwood Medical Industries. Device class: 2.

Clearance details

Applicant: Sherwood Medical Industries
Product code: Code BYI
Device class: Class 2
Regulation: 21 CFR 868.5665
Advisory panel: Anesthesiology
Date received: 1977-10-04
Decision date: 1977-10-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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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.