510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K897151Substantially Equivalent

Acuson V328 and C5432 Transducers

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

K897151 is the FDA 510(k) clearance record for ACUSON V328 AND C5432 TRANSDUCERS, a class I device, cleared for Acuson Corp. on under FDA product code JTX (Transport Systems, Anaerobic). FDA records list 37 510(k) clearances for Acuson Corp., from to . As of , FDA records show no recalls naming K897151.

Clearance record

Decision date
Received
(189 days to decision)
Product code
JTX Transport Systems, Anaerobic
Regulation
21 CFR 866.2900
Device class
Class I
Review panel
Microbiology
Applicant
Acuson Corp. 1220 Charleston Rd., Mountain View CA
Third party review
No

Clearances, product code JTX

Trailing 12 months

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

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