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

Knife, Tonsil

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

KBQ is the FDA product code for Knife, Tonsil, 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 no recalls.

Classification record

Product code
KBQ
Device name
Knife, Tonsil
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
0

Clearances, product code KBQ

By decision year
1 clearance under product code KBQ with a decision year between 1984 and 1984, 1984 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KBQ by decision year
YearClearances
19841

Applicants with the most clearances

Product code KBQ
Applicants holding the most 510(k) clearances under product code KBQ
ApplicantClearances
Premier Dental Products Co1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 47 companies shown, in name order