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

Brush, Cleaning, Tracheal Tube

21 CFR 868.5795 / Anesthesiology
FDA source (opens on fda.gov)

EPE is the FDA product code for Brush, Cleaning, Tracheal Tube, a class I device type, regulated under 21 CFR 868.5795. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
EPE
Device name
Brush, Cleaning, Tracheal Tube
Regulation
21 CFR 868.5795
Device class
Class I
Review panel
Anesthesiology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
2
Ingested recalls
1

Clearances, product code EPE

By decision year
2 clearances under product code EPE with a decision year between 1986 and 1986, 1986 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code EPE by decision year
YearClearances
19862

Applicants with the most clearances

Product code EPE
Applicants holding the most 510(k) clearances under product code EPE
ApplicantClearances
Biological & Environmental Control Laboratories1
Clinipad Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 66 companies shown, in name order