STRYKER LAPAROSCOPE— 510(k) K910132

Substantially Equivalent

Stryker Corp.

FDA 510(k) clearance K910132 for STRYKER LAPAROSCOPE, Substantially Equivalent on 1991-02-21. Applicant: Stryker Corp..

Clearance details

Applicant: Stryker Corp.
Product code: Code GCJ
Advisory panel: Gastroenterology, Urology
Date received: 1991-01-09
Decision date: 1991-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, US

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Adverse events under product code GCJ

product code GCJ

Death: 39
Injury: 1,638
Malfunction: 28,216
Other: 11
Total: 29,904

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.