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Tracheostomy And Nasal Suctioning Kit

Product code
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Device name
Tracheostomy And Nasal Suctioning Kit
Device class
Class 1
Medical specialty
Unknown
Marketing pathway
Enforcement Discretion
510(k) clearances (all years, FDA)
6 (all years; only the last 3 years are listed here)

FDA classification 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.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

Official FDA classification page: LRQ
Classification and pathway per current FDA publications. Data from openFDA (CC0).