CHRISTOUDIAS GAUZE DISSECTOR (LAPAROSCOPIC HAND INSTRUMENT)— 510(k) K982428

Substantially Equivalent

Innervision, Inc.

FDA 510(k) clearance K982428 for CHRISTOUDIAS GAUZE DISSECTOR (LAPAROSCOPIC HAND INSTRUMENT), Substantially Equivalent on 1998-10-09. Applicant: Innervision, Inc..

Clearance details

Applicant: Innervision, Inc.
Product code: Code HET
Advisory panel: Obstetrics/Gynecology
Date received: 1998-07-13
Decision date: 1998-10-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Memphis, TN, 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.