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LNZ — Changer, Tube, Endotracheal Class II

FDA Device Classification

Classification Details

Product Code
LNZ
Device Class
Class II
Regulation Number
868.5730
Submission Type
Review Panel
AN
Medical Specialty
Anesthesiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K102127instrumentation industriesENDOTRACHEAL TUBE CHANGERSAugust 27, 2010