SUR-FIT LOOP OSTOMY O.R. SET— 510(k) K811240

Substantially Equivalent

E. R. Squibb & Sons, Inc.

FDA 510(k) clearance K811240 for SUR-FIT LOOP OSTOMY O.R. SET, Substantially Equivalent on 1981-06-16. Applicant: E. R. Squibb & Sons, Inc..

Clearance details

Applicant: E. R. Squibb & Sons, Inc.
Product code: Code EXB
Advisory panel: Gastroenterology, Urology
Date received: 1981-05-04
Decision date: 1981-06-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

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Adverse events under product code EXB

product code EXB

Injury: 145
Total: 145

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.