DIPRIVAN LUER CONNECTOR— 510(k) K935274

Substantially Equivalent

Ohmeda Medical

FDA 510(k) clearance K935274 for DIPRIVAN LUER CONNECTOR, Substantially Equivalent on 1994-03-15. Applicant: Ohmeda Medical.

Clearance details

Applicant: Ohmeda Medical
Product code: Code LHI
Advisory panel: General Hospital
Date received: 1993-11-03
Decision date: 1994-03-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tampa, FL, 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.