510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K871727Substantially Equivalent

Modified Radius - Model Number Mm 5000

Ultrasonix, Inc., N. Yonkers NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K871727 is the FDA 510(k) clearance record for MODIFIED RADIUS - MODEL NUMBER MM 5000, a class II device, cleared for Ultrasonix, Inc. on under FDA product code JOP (Transducer, Ultrasonic). FDA records list 2 510(k) clearances for Ultrasonix, Inc., from to . As of , FDA records show no recalls naming K871727.

Clearance record

Decision date
Received
(155 days to decision)
Product code
JOP Transducer, Ultrasonic
Regulation
21 CFR 870.2880
Device class
Class II
Review panel
Cardiovascular
Applicant
Ultrasonix, Inc. 5 Odell Plz., N. Yonkers NY
Third party review
No

Clearances, product code JOP

Trailing 12 months

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

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