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

System, Intrafallopian Cannula

21 CFR 884.4530 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

MDG is the FDA product code for System, Intrafallopian Cannula, a class II device type, regulated under 21 CFR 884.4530. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
MDG
Device name
System, Intrafallopian Cannula
Regulation
21 CFR 884.4530
Device class
Class II
Review panel
Obstetrics/Gynecology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code MDG

By decision year
1 clearance under product code MDG with a decision year between 2000 and 2000, 2000 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MDG by decision year
YearClearances
20001

Applicants with the most clearances

Product code MDG
Applicants holding the most 510(k) clearances under product code MDG
ApplicantClearances
Medical Device Technologies, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code