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

Accessories, Cleaning Brushes, For Endoscope

21 CFR 876.1500 / Gastroenterology, Urology
FDA source (opens on fda.gov)

MNL is the FDA product code for Accessories, Cleaning Brushes, For Endoscope, a class I device type, regulated under 21 CFR 876.1500. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and 24 recalls.

Classification record

Product code
MNL
Device name
Accessories, Cleaning Brushes, For Endoscope
Regulation
21 CFR 876.1500
Device class
Class I
Review panel
Gastroenterology, Urology
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
24

Clearances, product code MNL

By decision year
4 clearances under product code MNL with a decision year between 1987 and 1995, 1995 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code MNL by decision year
YearClearances
19871
19891
19952

Applicants with the most clearances

Product code MNL
Applicants holding the most 510(k) clearances under product code MNL
ApplicantClearances
Endovations2
Cox Medical Ent., Inc.1
Mill-Rose Laboratory1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 210 companies shown, in name order