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

Check Valve, Retrograde Flow (In-Line)

21 CFR 880.5440 / General Hospital
FDA source (opens on fda.gov)

MJF is the FDA product code for Check Valve, Retrograde Flow (In-Line), a class II device type, regulated under 21 CFR 880.5440. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
MJF
Device name
Check Valve, Retrograde Flow (In-Line)
Regulation
21 CFR 880.5440
Device class
Class II
Review panel
General Hospital
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
1
Ingested recalls
0

Clearances, product code MJF

By decision year
1 clearance under product code MJF with a decision year between 1986 and 1986, 1986 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MJF by decision year
YearClearances
19861

Applicants with the most clearances

Product code MJF
Applicants holding the most 510(k) clearances under product code MJF
ApplicantClearances
Abbott Medical1

Companies listing this code with FDA

Companies whose registered establishments list this code