510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K910742Substantially Equivalent

Medi-Trace Disposable Intrauterine Catheter

Graphic Controls Corp., Buffalo NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K910742 is the FDA 510(k) clearance record for MEDI-TRACE DISPOSABLE INTRAUTERINE CATHETER, a class II device, cleared for Graphic Controls Corp. on under FDA product code KXO (Monitor, Pressure, Intrauterine). FDA records list 55 510(k) clearances for Graphic Controls Corp., from to . As of , FDA records show no recalls naming K910742.

Clearance record

Decision date
Received
(327 days to decision)
Product code
KXO Monitor, Pressure, Intrauterine
Regulation
21 CFR 884.2700
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Graphic Controls Corp. 189 Van Rensselaer St., Buffalo NY
Third party review
No

Clearances, product code KXO

Trailing 12 months

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

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