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

Loop, Wire

21 CFR 874.4420 / Ear, Nose, Throat
FDA source (opens on fda.gov)

JYQ is the FDA product code for Loop, Wire, a class I device type, regulated under 21 CFR 874.4420. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JYQ
Device name
Loop, Wire
Regulation
21 CFR 874.4420
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
2
Ingested recalls
0

Clearances, product code JYQ

By decision year
2 clearances under product code JYQ with a decision year between 1987 and 1989, 1987 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JYQ by decision year
YearClearances
19871
19891

Applicants with the most clearances

Product code JYQ
Applicants holding the most 510(k) clearances under product code JYQ
ApplicantClearances
Kinetic Medical Products1
Treace Medical, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 84 companies shown, in name order