PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICES— 510(k) K994151

Substantially Equivalent

Ximed/Prosure/Injectx

FDA 510(k) clearance K994151 for PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICES, Substantially Equivalent on 2000-03-01. Applicant: Ximed/Prosure/Injectx.

Clearance details

Applicant: Ximed/Prosure/Injectx
Product code: Code GAA
Advisory panel: General, Plastic Surgery
Date received: 1999-12-09
Decision date: 2000-03-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Jose, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code GAA

product code GAA

Malfunction: 834
Total: 834

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.