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

Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Sterile

21 CFR 872.6855 / Dental
FDA source (opens on fda.gov)

MCF is the FDA product code for Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Sterile, a class I device type, regulated under 21 CFR 872.6855. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
MCF
Device name
Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Sterile
Regulation
21 CFR 872.6855
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
5
Ingested recalls
1

Clearances, product code MCF

By decision year
5 clearances under product code MCF with a decision year between 1990 and 2003, 1990 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code MCF by decision year
YearClearances
19902
20011
20021
20031

Applicants with the most clearances

Product code MCF
Applicants holding the most 510(k) clearances under product code MCF
ApplicantClearances
Associated Mills, Inc.1
Germ Terminator Corporation1
Hwadong International Company, Ltd.1
Otres, LLC1
Purebrush Assoc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 15 companies shown, in name order