ILLINOIS STERNAL/ILIAC ASPIRATION NEEDLE— 510(k) K930160

Substantially Equivalent

Symbiosis Corp.

FDA 510(k) clearance K930160 for ILLINOIS STERNAL/ILIAC ASPIRATION NEEDLE, Substantially Equivalent on 1993-07-06. Applicant: Symbiosis Corp..

Clearance details

Applicant: Symbiosis Corp.
Product code: Code GDM
Advisory panel: General, Plastic Surgery
Date received: 1993-01-13
Decision date: 1993-07-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code GDM

product code GDM

Death: 2
Total: 2

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.