TECHNOFIL— 510(k) K953748

Substantially Equivalent

Technimeca Medic, Inc.

FDA 510(k) clearance K953748 for TECHNOFIL, Substantially Equivalent on 1996-01-25. Applicant: Technimeca Medic, Inc..

Clearance details

Applicant: Technimeca Medic, Inc.
Product code: Code CAD
Advisory panel: Anesthesiology
Date received: 1995-08-11
Decision date: 1996-01-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Laurent, Quebec, CA

Download summary PDF View on FDA.gov ↗

Adverse events under product code CAD

product code CAD

Malfunction: 3,275
Total: 3,275

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.