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

Washer, Endometrial

21 CFR 884.1185 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

HFD is the FDA product code for Washer, Endometrial, a class II device type, regulated under 21 CFR 884.1185. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HFD
Device name
Washer, Endometrial
Regulation
21 CFR 884.1185
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
Yes
Ingested clearances
3
Ingested recalls
0

Clearances, product code HFD

By decision year
3 clearances under product code HFD with a decision year between 1981 and 1989, 1989 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code HFD by decision year
YearClearances
19811
19892

Applicants with the most clearances

Product code HFD
Applicants holding the most 510(k) clearances under product code HFD
ApplicantClearances
Associated Medical Products Co.1
Kinetic Medical Products1
Zinnanti Surgical Instruments, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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