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

Snare, Ear

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

JZD is the FDA product code for Snare, Ear, 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
JZD
Device name
Snare, Ear
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 JZD

By decision year
2 clearances under product code JZD with a decision year between 1982 and 1983, 1982 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JZD by decision year
YearClearances
19821
19831

Applicants with the most clearances

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

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 33 companies shown, in name order