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

Prosthesis, Fallopian Tube

21 CFR 884.3650 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

HFJ is the FDA product code for Prosthesis, Fallopian Tube, a class II device type, regulated under 21 CFR 884.3650. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
HFJ
Device name
Prosthesis, Fallopian Tube
Regulation
21 CFR 884.3650
Device class
Class II
Review panel
Obstetrics/Gynecology
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code HFJ

By decision year
1 clearance under product code HFJ with a decision year between 1994 and 1994, 1994 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HFJ by decision year
YearClearances
19941

Applicants with the most clearances

Product code HFJ
Applicants holding the most 510(k) clearances under product code HFJ
ApplicantClearances
Cook Ob/Gyn1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code HFJ.