CONVENIENCE CONTOUR KITS REDI NURSE SYSTEM— 510(k) K935092

Unknown

Contour Fabricators of Florida, Inc.

FDA 510(k) clearance K935092 for CONVENIENCE CONTOUR KITS REDI NURSE SYSTEM, Unknown on 1994-06-10. Applicant: Contour Fabricators of Florida, Inc..

Clearance details

Applicant: Contour Fabricators of Florida, Inc.
Product code: Code FMF
Advisory panel: General Hospital
Date received: 1993-10-25
Decision date: 1994-06-10
Decision: Unknown
Clearance type: Traditional
Location: St. Petersburg, FL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FMF

product code FMF

Death: 15
Injury: 2,263
Malfunction: 29,722
Other: 17
Total: 32,017

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.