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

Splint, Intranasal Septal, Cber Led

21 CFR 874.4780 / Ear, Nose, Throat
FDA source (opens on fda.gov)

QJL is the FDA product code for Splint, Intranasal Septal, Cber Led, a class I device type, regulated under 21 CFR 874.4780. FDA's definition for this code reads: "Splint, Intranasal Septal, CBER led". As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
QJL
Device name
Splint, Intranasal Septal, Cber Led
FDA definition
Splint, Intranasal Septal, CBER led
Regulation
21 CFR 874.4780
Device class
Class I
Review panel
Ear, Nose, Throat
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code QJL

By decision year
1 clearance under product code QJL with a decision year between 2016 and 2016, 2016 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code QJL by decision year
YearClearances
20161

Applicants with the most clearances

Product code QJL
Applicants holding the most 510(k) clearances under product code QJL
ApplicantClearances
Bioinspire Technologies, Incorporated1

Companies listing this code with FDA

Companies whose registered establishments list this code