510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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LNZClass II

Changer, Tube, Endotracheal

21 CFR 868.5730 / Anesthesiology
FDA source (opens on fda.gov)

LNZ is the FDA product code for Changer, Tube, Endotracheal, a class II device type, regulated under 21 CFR 868.5730. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and 3 recalls.

Classification record

Product code
LNZ
Device name
Changer, Tube, Endotracheal
Regulation
21 CFR 868.5730
Device class
Class II
Review panel
Anesthesiology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
1
Ingested recalls
3

Clearances, product code LNZ

By decision year
1 clearance under product code LNZ with a decision year between 2010 and 2010, 2010 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LNZ by decision year
YearClearances
20101

Applicants with the most clearances

Product code LNZ
Applicants holding the most 510(k) clearances under product code LNZ
ApplicantClearances
Instrumentation Industries, Incorporated1

Companies listing this code with FDA

Companies whose registered establishments list this code