510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K930964Substantially Equivalent

Acuson Model #29001 (Diagnostic Ultrasound Device)

Acuson Corp., Mountain View CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930964 is the FDA 510(k) clearance record for ACUSON MODEL #29001 (DIAGNOSTIC ULTRASOUND DEVICE), a class II device, cleared for Acuson Corp. on under FDA product code IYO (System, Imaging, Pulsed Echo, Ultrasonic). FDA records list 37 510(k) clearances for Acuson Corp., from to . As of , FDA records show no recalls naming K930964.

Clearance record

Decision date
Received
(609 days to decision)
Product code
IYO System, Imaging, Pulsed Echo, Ultrasonic
Regulation
21 CFR 892.1560
Device class
Class II
Review panel
Radiology
Applicant
Acuson Corp. 1220 Charleston Rd., Mountain View CA
510(k) summary
Summary
Third party review
No

Clearances, product code IYO

Trailing 12 months
8 clearances under product code IYO in the twelve months to October 2026, February 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code IYO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20262
March 20261
April 20262
May 20260
June 20261
July 20261
August 20260
September 20261
October 20260