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

Curette, Surgical, Dental

21 CFR 872.4565 / Dental
FDA source (opens on fda.gov)

EMK is the FDA product code for Curette, Surgical, Dental, a class I device type, regulated under 21 CFR 872.4565. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
EMK
Device name
Curette, Surgical, Dental
Regulation
21 CFR 872.4565
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
1
Ingested recalls
0

Clearances, product code EMK

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

Applicants with the most clearances

Product code EMK
Applicants holding the most 510(k) clearances under product code EMK
ApplicantClearances
Artiberia1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 125 companies shown, in name order