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

Nipper, Malleus

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

JYR is the FDA product code for Nipper, Malleus, 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
JYR
Device name
Nipper, Malleus
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 JYR

By decision year
2 clearances under product code JYR with a decision year between 1979 and 1982, 1979 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JYR by decision year
YearClearances
19791
19821

Applicants with the most clearances

Product code JYR
Applicants holding the most 510(k) clearances under product code JYR
ApplicantClearances
Kelleher Corp.1
Xomed, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 66 companies shown, in name order