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

Tube, Ear Suction

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

JZF is the FDA product code for Tube, Ear Suction, a class I device type, regulated under 21 CFR 874.4420. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JZF
Device name
Tube, Ear Suction
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
5
Ingested recalls
0

Clearances, product code JZF

By decision year
5 clearances under product code JZF with a decision year between 1982 and 1998, 1982 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JZF by decision year
YearClearances
19821
19841
19851
19861
19981

Applicants with the most clearances

Product code JZF
Applicants holding the most 510(k) clearances under product code JZF
ApplicantClearances
Downs Surgical, Ltd.1
Exmoor Plastics Limited1
Kelleher Corp.1
Steven K. Juhn1
Treace Medical, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 138 companies shown, in name order