GETTIG UNIVERSAL VIAL ACCESS PIN— 510(k) K041232

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..

Clearance details

Applicant: Gettig Pharmaceutical Instrument Co.
Product code: Code LHI
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

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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.