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

Tube Impression And Matrix

21 CFR 872.6570 / Dental
FDA source (opens on fda.gov)

KCQ is the FDA product code for Tube Impression And Matrix, a class I device type, regulated under 21 CFR 872.6570. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
KCQ
Device name
Tube Impression And Matrix
Regulation
21 CFR 872.6570
Device class
Class I
Review panel
Dental
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code KCQ

By decision year
1 clearance under product code KCQ with a decision year between 1990 and 1990, 1990 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KCQ by decision year
YearClearances
19901

Applicants with the most clearances

Product code KCQ
Applicants holding the most 510(k) clearances under product code KCQ
ApplicantClearances
Intl. Medical Marketing, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 23 companies shown, in name order