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
KBCClass I

Saw, Nasal

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

KBC is the FDA product code for Saw, Nasal, a class I device type, regulated under 21 CFR 874.4420. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KBC
Device name
Saw, Nasal
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
4
Ingested recalls
0

Clearances, product code KBC

By decision year
4 clearances under product code KBC with a decision year between 1978 and 1981, 1981 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code KBC by decision year
YearClearances
19781
19813

Applicants with the most clearances

Product code KBC
Applicants holding the most 510(k) clearances under product code KBC
ApplicantClearances
United States Surgical, A Division of Tyco Healthc2
Edward Weck, Inc.1
Sierra Laboratories, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 58 companies shown, in name order