GAUZE & LAB SPONGES STERILE & NON— 510(k) K842572

Substantially Equivalent

Ulti-Med Intl., Inc.

FDA 510(k) clearance K842572 for GAUZE & LAB SPONGES STERILE & NON, Substantially Equivalent on 1984-08-15. Applicant: Ulti-Med Intl., Inc..

Clearance details

Applicant: Ulti-Med Intl., Inc.
Product code: Code GDY
Advisory panel: General, Plastic Surgery
Date received: 1984-07-03
Decision date: 1984-08-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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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.