510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K162667Substantially Equivalent

Kitazato IUI Catheter

Kitazato Corporation, Tokyo, JP / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K162667 is the FDA 510(k) clearance record for Kitazato IUI Catheter, a class II device, cleared for Kitazato Corporation on under FDA product code MQF (Catheter, Assisted Reproduction). FDA records list 13 510(k) clearances for Kitazato Corporation, from to . As of , FDA records show no recalls naming K162667.

Clearance record

Decision date
Received
(227 days to decision)
Product code
MQF Catheter, Assisted Reproduction
Regulation
21 CFR 884.6110
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Kitazato Corporation 1-1-8 Shibadaimon, Minato-Ku, Tokyo, JP
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MQF

Trailing 12 months
1 clearance under product code MQF in the twelve months to October 2026, February 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MQF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260