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

Device, Engorgement, Clitoral

21 CFR 884.5970 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

NBV is the FDA product code for Device, Engorgement, Clitoral, a class II device type, regulated under 21 CFR 884.5970. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
NBV
Device name
Device, Engorgement, Clitoral
Regulation
21 CFR 884.5970
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
No
Ingested clearances
3
Ingested recalls
0

Clearances, product code NBV

By decision year
3 clearances under product code NBV with a decision year between 2000 and 2005, 2000 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code NBV by decision year
YearClearances
20002
20051

Applicants with the most clearances

Product code NBV
Applicants holding the most 510(k) clearances under product code NBV
ApplicantClearances
Gynavations, Inc.1
Prosurg, Inc1
Urometrics, 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 NBV.