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

Tube, Tonsil Suction

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

KCB is the FDA product code for Tube, Tonsil Suction, a class I device type, regulated under 21 CFR 874.4420. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and one recall.

Classification record

Product code
KCB
Device name
Tube, Tonsil 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
1
Ingested recalls
1

Clearances, product code KCB

By decision year
1 clearance under product code KCB with a decision year between 1980 and 1980, 1980 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KCB by decision year
YearClearances
19801

Applicants with the most clearances

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

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 105 companies shown, in name order