MEDIFIX SINGLE AND DOUBLE PUNCTURE LAPAROSCOPES— 510(k) K992480

Substantially Equivalent

Medifix, Inc.

FDA 510(k) clearance K992480 for MEDIFIX SINGLE AND DOUBLE PUNCTURE LAPAROSCOPES, Substantially Equivalent on 1999-09-23. Applicant: Medifix, Inc..

Clearance details

Applicant: Medifix, Inc.
Product code: Code HET
Advisory panel: Obstetrics/Gynecology
Date received: 1999-07-26
Decision date: 1999-09-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Morton Grove, IL, 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.