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

Elevator, Uterine

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

HDP is the FDA product code for Elevator, Uterine, a class II device type, regulated under 21 CFR 884.4530. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HDP
Device name
Elevator, Uterine
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
Yes
Ingested clearances
4
Ingested recalls
0

Clearances, product code HDP

By decision year
4 clearances under product code HDP with a decision year between 1982 and 1998, 1998 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code HDP by decision year
YearClearances
19821
19881
19982

Applicants with the most clearances

Product code HDP
Applicants holding the most 510(k) clearances under product code HDP
ApplicantClearances
Bivona Medical Technologies1
Clinical Innovations, LLC1
Conkin Surgical Instruments Ltd.1
Zinnanti Surgical Instruments, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code