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

Viscometer, Mucus, Cervical

21 CFR 884.1040 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

LHZ is the FDA product code for Viscometer, Mucus, Cervical, a class I device type, regulated under 21 CFR 884.1040. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
LHZ
Device name
Viscometer, Mucus, Cervical
Regulation
21 CFR 884.1040
Device class
Class I
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 LHZ

By decision year
1 clearance under product code LHZ with a decision year between 1996 and 1996, 1996 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LHZ by decision year
YearClearances
19961

Applicants with the most clearances

Product code LHZ
Applicants holding the most 510(k) clearances under product code LHZ
ApplicantClearances
Harold J. Kosasky, M.D.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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