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

Vaginoscope And Accessories

21 CFR 884.1630 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

MOK is the FDA product code for Vaginoscope And Accessories, a class II device type, regulated under 21 CFR 884.1630. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MOK
Device name
Vaginoscope And Accessories
Regulation
21 CFR 884.1630
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
2
Ingested recalls
0

Clearances, product code MOK

By decision year
2 clearances under product code MOK with a decision year between 1995 and 2022, 1995 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MOK by decision year
YearClearances
19951
20221

Applicants with the most clearances

Product code MOK
Applicants holding the most 510(k) clearances under product code MOK
ApplicantClearances
Applied Medical Resources Corp1
Karl Storz Endoscopy-America, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code