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

Trocar, Sinus

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

KBG is the FDA product code for Trocar, Sinus, a class I device type, regulated under 21 CFR 874.4420. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KBG
Device name
Trocar, Sinus
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
3
Ingested recalls
0

Clearances, product code KBG

By decision year
3 clearances under product code KBG with a decision year between 1985 and 2005, 1985 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KBG by decision year
YearClearances
19851
20021
20051

Applicants with the most clearances

Product code KBG
Applicants holding the most 510(k) clearances under product code KBG
ApplicantClearances
Adven Medical1
Chesebrough-Pond'S U.S.A. Co.1
Clearmedical, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 22 companies shown, in name order