OJA

1 FDA 510(k) clearances · Product code

FDA profile

Official device name

Intravenous Extension Tubing Set

Device class

Class II (moderate risk)

Regulation

21 CFR 880.5440

Medical specialty

General Hospital

FDA definition

This product code has been established in accordance with the May 20, 1997, Guidance entitled, Convenience Kits Interim Regulatory Guidance, found at www.fda.gov/cdrh/ode/convkit.html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.

Adverse events (MAUDE)

2009: 3
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.

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