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

Drain, Cervical

21 CFR 884.3200 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

HFL is the FDA product code for Drain, Cervical, a class II device type, regulated under 21 CFR 884.3200. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
HFL
Device name
Drain, Cervical
Regulation
21 CFR 884.3200
Device class
Class II
Review panel
Obstetrics/Gynecology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code HFL

By decision year
1 clearance under product code HFL with a decision year between 1991 and 1991, 1991 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HFL by decision year
YearClearances
19911

Applicants with the most clearances

Product code HFL
Applicants holding the most 510(k) clearances under product code HFL
ApplicantClearances
Sil-Med Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code