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

Catheters, Salpingography

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

MOV is the FDA product code for Catheters, Salpingography, a class II device type, regulated under 21 CFR 884.4530. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and 3 recalls.

Classification record

Product code
MOV
Device name
Catheters, Salpingography
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
5
Ingested recalls
3

Clearances, product code MOV

By decision year
5 clearances under product code MOV with a decision year between 1995 and 2018, 1995 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code MOV by decision year
YearClearances
19954
20181

Applicants with the most clearances

Product code MOV
Applicants holding the most 510(k) clearances under product code MOV
ApplicantClearances
Conceptus, Inc.1
Cook Incorporated1
Cook Ob/Gyn1
Echocath, Inc.1
Ovamed Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code