510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K961002Substantially Equivalent

Diasonics Itnraoperative Probes

Diasonics Ultrasound, Santa Clara CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K961002 is the FDA 510(k) clearance record for DIASONICS ITNRAOPERATIVE PROBES, a class II device, cleared for Diasonics Ultrasound on under FDA product code ITX (Transducer, Ultrasonic, Diagnostic). FDA records list 2 510(k) clearances for Diasonics Ultrasound, from to . As of , FDA records show no recalls naming K961002.

Clearance record

Decision date
Received
(316 days to decision)
Product code
ITX Transducer, Ultrasonic, Diagnostic
Regulation
21 CFR 892.1570
Device class
Class II
Review panel
Radiology
Applicant
Diasonics Ultrasound 2860 Dela Cruz Blvd., Santa Clara CA
510(k) summary
Statement
Third party review
No

Clearances, product code ITX

Trailing 12 months
6 clearances under product code ITX in the twelve months to October 2026, July 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code ITX, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20263
August 20262
September 20261
October 20260