510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K905728Substantially Equivalent

Sonos 500 and Sonos 1000 Ultrasound Imaging System

Hewlett-Packard Co., Andover MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K905728 is the FDA 510(k) clearance record for SONOS 500 AND SONOS 1000 ULTRASOUND IMAGING SYSTEM, a class II device, cleared for Hewlett-Packard Co. on under FDA product code DPT (Probe, Blood-Flow, Extravascular). FDA records list 246 510(k) clearances for Hewlett-Packard Co., from to . As of , FDA records show no recalls naming K905728.

Clearance record

Decision date
Received
(81 days to decision)
Product code
DPT Probe, Blood-Flow, Extravascular
Regulation
21 CFR 870.2120
Device class
Class II
Review panel
Cardiovascular
Applicant
Hewlett-Packard Co. 3000 Minuteman Rd., Andover MA
Third party review
No

Clearances, product code DPT

Trailing 12 months

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

FDA records show no clearances under product code DPT in the twelve months to November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DPT, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260