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

Cannula, Intrauterine Insemination

21 CFR 884.5250 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

MFD is the FDA product code for Cannula, Intrauterine Insemination, a class II device type, regulated under 21 CFR 884.5250. As of , FDA records hold 29 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
MFD
Device name
Cannula, Intrauterine Insemination
Regulation
21 CFR 884.5250
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
29
Ingested recalls
1

Clearances, product code MFD

By decision year
29 clearances under product code MFD with a decision year between 1991 and 2002, 1995 the highest year at 5.
Show the numbers
510(k) clearances under FDA product code MFD by decision year
YearClearances
19913
19921
19934
19943
19955
19963
19974
19982
19992
20011
20021

Applicants with the most clearances

Product code MFD
Applicants holding the most 510(k) clearances under product code MFD
ApplicantClearances
Life-Tech Intl., Inc.4
A & A Medical, Inc.2
Cook Ob/Gyn2
Life Technologies Corporation2
Marlo Surgical Technology2
Medworks Corp.2
Select Medical Systems, Inc.2
Ackrad Laboratories1
Conceptus, Inc.1
Cook Incorporated1

Companies listing this code with FDA

Companies whose registered establishments list this code