CONTAIN X-RAY DETECTABLE LAP SPONGE— 510(k) K801768

Name: FDA 510(k) clearance K801768
Creator: U.S. Food and Drug Administration
Published: 1980-08-20

Substantially Equivalent

The Buckeye Cellulose Corp.

FDA 510(k) clearance K801768 for CONTAIN X-RAY DETECTABLE LAP SPONGE, Substantially Equivalent on 1980-08-20. Applicant: The Buckeye Cellulose Corp.. Device class: 1.

Clearance details

Applicant: The Buckeye Cellulose Corp.
Product code: Code GDY
Device class: Class 1
Regulation: 21 CFR 878.4450
Advisory panel: General, Plastic Surgery
Date received: 1980-07-28
Decision date: 1980-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K821564 — BOUNDARY PROCESS CHANGE1982-07-02
K820758 — BOUNDARY SINGLE-USE CRANIOTOMY SHEET1982-04-29
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Adverse events under product code GDY

product code GDY

Malfunction: 764
Total: 764

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.