510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K953314Substantially Equivalent

Conceptus Fallopian Tube Catheterization System

Conceptus, Inc., San Carlos CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K953314 is the FDA 510(k) clearance record for CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM, a class II device, cleared for Conceptus, Inc. on under FDA product code MOV (Catheters, Salpingography). FDA records list 9 510(k) clearances for Conceptus, Inc., from to . As of , FDA records show no recalls naming K953314.

Clearance record

Decision date
Received
(16 days to decision)
Product code
MOV Catheters, Salpingography
Regulation
21 CFR 884.4530
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Conceptus, Inc. 1021 Howard Ave., San Carlos CA
510(k) summary
Statement
Third party review
No

Clearances, product code MOV

Trailing 12 months

FDA records hold no clearances under product code MOV in the trailing twelve months.

FDA records show no clearances under product code MOV in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MOV, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260