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

Gauge, Measuring

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

JYJ is the FDA product code for Gauge, Measuring, 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
JYJ
Device name
Gauge, Measuring
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 JYJ

By decision year
5 clearances under product code JYJ with a decision year between 1980 and 1991, 1980 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JYJ by decision year
YearClearances
19801
19841
19881
19891
19911

Applicants with the most clearances

Product code JYJ
Applicants holding the most 510(k) clearances under product code JYJ
ApplicantClearances
Suredrop, Inc.2
Aztec Medical Products, Inc.1
Kc Medical Industries1
Microtek Medical LLC1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 65 companies shown, in name order