510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K860313Substantially Equivalent

3.0 Mhz Linear Array Probe Model Ust 5031

Johnson & Johnson Professionals, Inc., Ramsey NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K860313 is the FDA 510(k) clearance record for 3.0 MHZ LINEAR ARRAY PROBE MODEL UST 5031, a class II device, cleared for Johnson & Johnson Professionals, Inc. on under FDA product code HGL (Transducer, Ultrasonic, Obstetric). FDA records list 206 510(k) clearances for Johnson & Johnson Professionals, Inc., from to . As of , FDA records show no recalls naming K860313.

Clearance record

Decision date
Received
(48 days to decision)
Product code
HGL Transducer, Ultrasonic, Obstetric
Regulation
21 CFR 884.2960
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Johnson & Johnson Professionals, Inc. 69 Spring St., Ramsey NJ
Third party review
No

Clearances, product code HGL

Trailing 12 months

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

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