HI-TEMP LOOPTIP SURGICAL CAUTERY— 510(k) K802330

Substantially Equivalent

Medical Products Development, Inc.

FDA 510(k) clearance K802330 for HI-TEMP LOOPTIP SURGICAL CAUTERY, Substantially Equivalent on 1980-11-12. Applicant: Medical Products Development, Inc..

Clearance details

Applicant: Medical Products Development, Inc.
Product code: Code GEI
Advisory panel: General, Plastic Surgery
Date received: 1980-09-23
Decision date: 1980-11-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code GEI

product code GEI

Death: 133
Injury: 7,585
Malfunction: 35,808
Other: 44
Total: 43,570

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.