LAPAROSCOPIC TROCAR— 510(k) K911483

Name: FDA 510(k) clearance K911483
Creator: U.S. Food and Drug Administration
Published: 1991-07-02

Substantially Equivalent

United States Endoscopy Group, Inc.

FDA 510(k) clearance K911483 for LAPAROSCOPIC TROCAR, Substantially Equivalent on 1991-07-02. Applicant: United States Endoscopy Group, Inc.. Device class: 2.

Clearance details

Applicant: United States Endoscopy Group, Inc.
Product code: Code DRC
Device class: Class 2
Regulation: 21 CFR 870.1390
Advisory panel: Cardiovascular
Date received: 1991-04-04
Decision date: 1991-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mentor, OH, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code DRC

product code DRC

Death: 28
Injury: 412
Total: 440

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.