510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K905563Substantially Equivalent

Intran Plus

Utah Medical Products, Inc, Midvale UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K905563 is the FDA 510(k) clearance record for INTRAN PLUS, a class II device, cleared for Utah Medical Products, Inc. on under FDA product code KXO (Monitor, Pressure, Intrauterine). FDA records list 38 510(k) clearances for Utah Medical Products, Inc., from to . As of , FDA records show one recall naming K905563.

Clearance record

Decision date
Received
(189 days to decision)
Product code
KXO Monitor, Pressure, Intrauterine
Regulation
21 CFR 884.2700
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Utah Medical Products, Inc. 7043 S. 300 W., Midvale UT
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