510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K140761Substantially Equivalent

Kahn Uterine Cannula, Jarcho Uterine Cannula, Neal Fallopian Cannula

Medtronic, Inc., Vernon Hills IL / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K140761 is the FDA 510(k) clearance record for KAHN UTERINE CANNULA, JARCHO UTERINE CANNULA, NEAL FALLOPIAN CANNULA, a class II device, cleared for Carefusion 2200, Inc. on under FDA product code HES (Insufflator, Carbon-Dioxide, Uterotubal (And Accessories)). FDA records list 1,525 510(k) clearances for Medtronic, Inc., from to . As of , FDA records show no recalls naming K140761.

Clearance record

Decision date
Received
(26 days to decision)
Product code
HES Insufflator, Carbon-Dioxide, Uterotubal (And Accessories)
Regulation
21 CFR 884.1300
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Carefusion 2200, Inc. 72 N. Fairway Dr., Vernon Hills IL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HES

Trailing 12 months

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

FDA records show no clearances under product code HES in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HES, 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