SMITH & NEPHEW DYONICS MICROLAPAROSCOPE— 510(k) K982149

Substantially Equivalent

Smith & Nephew, Inc.

FDA 510(k) clearance K982149 for SMITH & NEPHEW DYONICS MICROLAPAROSCOPE, Substantially Equivalent on 1998-09-10. Applicant: Smith & Nephew, Inc..

Clearance details

Applicant: Smith & Nephew, Inc.
Product code: Code HET
Advisory panel: Obstetrics/Gynecology
Date received: 1998-06-18
Decision date: 1998-09-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Andover, MA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code HET

product code HET

Malfunction: 10,504
Total: 10,504

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.