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

Adhesive, Denture, Carboxymethylcellulose Sodium (40-100&)

21 CFR 872.3410 / Dental
FDA source (opens on fda.gov)

KOQ is the FDA product code for Adhesive, Denture, Carboxymethylcellulose Sodium (40-100&), a class I device type, regulated under 21 CFR 872.3410. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KOQ
Device name
Adhesive, Denture, Carboxymethylcellulose Sodium (40-100&)
Regulation
21 CFR 872.3410
Device class
Class I
Review panel
Dental
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 KOQ

By decision year
4 clearances under product code KOQ with a decision year between 1983 and 1990, 1990 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code KOQ by decision year
YearClearances
19831
19903

Applicants with the most clearances

Product code KOQ
Applicants holding the most 510(k) clearances under product code KOQ
ApplicantClearances
North American Sterilization & Packaging Co.2
Solar Dental Co., Inc.1
Uresil, LLC1

Companies listing this code with FDA

Companies whose registered establishments list this code