GETTIG UNIVERSAL VIAL ACCESS PIN— 510(k) K041232

Name: FDA 510(k) clearance K041232
Creator: U.S. Food and Drug Administration
Published: 2004-07-22

Substantially Equivalent

Gettig Pharmaceutical Instrument Co.

FDA 510(k) clearance K041232 for GETTIG UNIVERSAL VIAL ACCESS PIN, Substantially Equivalent on 2004-07-22. Applicant: Gettig Pharmaceutical Instrument Co.. Device class: 2.

Clearance details

Applicant: Gettig Pharmaceutical Instrument Co.
Product code: Code LHI
Device class: Class 2
Regulation: 21 CFR 880.5440
Advisory panel: General Hospital
Date received: 2004-05-10
Decision date: 2004-07-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Spring Mills, PA, US

Download summary PDF View on FDA.gov ↗

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K033409 — AMERSHAM HEALTH NEEDLE-GUARD2004-01-21
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K000455 — GETTIG GUARD2000-04-19
K972285 — GETTIG STYRL-JECT DELIVERY SYSTEM1997-09-11

Adverse events under product code LHI

product code LHI

Injury: 207
Malfunction: 7,820
Other: 3
Total: 8,030

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.