UNIVEC AUTO-DISABLE HYPODERMIC SYRINGE— 510(k) K993996

Name: FDA 510(k) clearance K993996
Creator: U.S. Food and Drug Administration
Published: 2000-07-17

Substantially Equivalent

Univec, Inc.

FDA 510(k) clearance K993996 for UNIVEC AUTO-DISABLE HYPODERMIC SYRINGE, Substantially Equivalent on 2000-07-17. Applicant: Univec, Inc.. Device class: 2.

Clearance details

Applicant: Univec, Inc.
Product code: Code MEG
Device class: Class 2
Regulation: 21 CFR 880.5860
Advisory panel: General Hospital
Date received: 1999-11-24
Decision date: 2000-07-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Farmingdale, NY, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code MEG

product code MEG

Malfunction: 1,373
Other: 1
Total: 1,374

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.