510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
JYCClass I

Cannula, Ear

21 CFR 878.4800 / General, Plastic Surgery
FDA source (opens on fda.gov)

JYC is the FDA product code for Cannula, Ear, a class I device type, regulated under 21 CFR 878.4800. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JYC
Device name
Cannula, Ear
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
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 JYC

By decision year
2 clearances under product code JYC with a decision year between 1978 and 1989, 1978 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JYC by decision year
YearClearances
19781
19891

Applicants with the most clearances

Product code JYC
Applicants holding the most 510(k) clearances under product code JYC
ApplicantClearances
Edward Weck, Inc.1
Syva Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 49 companies shown, in name order