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

Device, Fertility Diagnostic, Proceptive

Unknown
FDA source (opens on fda.gov)

LHD is the FDA product code for Device, Fertility Diagnostic, Proceptive. As of , FDA records hold 24 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LHD
Device name
Device, Fertility Diagnostic, Proceptive
Device class
Unclassified
Review panel
Unknown
Submission type
FDA code 7
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
24
Ingested recalls
0

Clearances, product code LHD

By decision year
24 clearances under product code LHD with a decision year between 1981 and 2021, 1985 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code LHD by decision year
YearClearances
19811
19822
19832
19841
19854
19872
19881
19901
19921
19952
20011
20032
20061
20111
20131
20211

Applicants with the most clearances

Product code LHD
Applicants holding the most 510(k) clearances under product code LHD
ApplicantClearances
Bioself, Inc.3
Nishitomo Co., Inc.2
Ava AG1
BD Becton Dickinson Vacutainer Systems Preanalytic1
Cambridge Temperature Concepts, Ltd.1
Fertil-A-Chron, Inc.1
Fertile Time, Ltd.1
Fertility Focus, Ltd.1
Forecaster Co.1
Joel R.L. Ehren Kranz1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 29 companies shown, in name order