Sonos 500 and Sonos 1000 Ultrasound Imaging System

FDA 510(k) K905728 · Hewlett-Packard Co.

Substantially Equivalent

510(k) numberK905728

Submission

Device name
Sonos 500 and Sonos 1000 Ultrasound Imaging System
Applicant
Hewlett-Packard Co.
Andover, MA, US
Received
December 24, 1990
Decision date
March 15, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DPT – Probe, Blood-Flow, Extravascular
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2120
Specialty
Cardiovascular

Other 510(k)s with product code DPT

510(k)DeviceApplicantDecision
K233076Laser Speckle Imaging System (RFLSI CZW)DPT · Traditional Rwd Life Science Co., Ltd.05/28/2024SE
K163339Spectralmd Deepview Wound Imaging System 2.0DPT · Traditional Spectralmd, Inc.08/17/2017SE
K152749moorLDI2-IR Infrared laser Doppler imager, moorLDI2-HIR High Resolution Infrared laser…DPT · Traditional Moor Instruments, Ltd.05/12/2016SE
K142932Deltex Medical KDP72 Doppler ProbeDPT · Traditional Deltex Medical Limited01/22/2015SE
K132730Bio-Probe Disposable Insert with; Balance Biosurface, Carmeda Bioactive Surface…DPT · Traditional Medtronic, Inc.05/30/2014SE
K133903Bio-Probe Transducer (Adult)DPT · Traditional Medtronic, Inc.04/10/2014SE
K132163Moorldls-Bi Laser Doppler Burns ImagerDPT · Traditional Moor Instruments, Ltd.01/29/2014SE
K124049Deepview Digital Video Physiological Portable Imaging SystemDPT · Traditional Spectralmd, Inc.04/18/2013SE
K123216Aimago Easyldi Microcirculation Camera (Stand Plus Camera Arm), Aimago Easy Ldi Stand…DPT · Traditional Aimago SA02/07/2013SE
K122943MOORFLPI-2 Full-Field Laser Perfusion ImagerDPT · Traditional Moor Instruments, Ltd.01/03/2013SE

More from Moor Instruments, Ltd.

510(k)DeviceDecision
K992543Heartstream XLT Defibrillator/Monitor, Ac Charger, DC Charger, Data Card, Single Bay…MKJ · Traditional 05/18/2000SE
K993383HP Viridia Multi-Measurement Server/Compact Portable Patient Monitor Models M3000A…DSI · Abbreviated 02/03/2000SE
K992273HP Viridia Multi-Measurement Server/Compact Portable Patient Monitor…MHX · Abbreviated 01/28/2000SE
K993587HP M2376A Device Link SystemMQS · Traditional 01/20/2000SE
K993169Modification of: Physiological Signal Transmitter and Receiver, Model 3810ADRG · Traditional 12/20/1999SE
K992595HP Viridia Component Monitoring System, Model Rev. K with Easi-St Segment Measurement…MHX · Special 12/08/1999SE
K992977Hewlett Packard Multifunction Pediatric Defib Function, Model M3503A & M3504AMKJ · Traditional 12/01/1999SE
K993516HP M2600A Viridia Telemetry SystemDSI · Special 11/08/1999SE
K992674HP Viridia CMS Patient Monitor with EEG Parameter, Model M1027AMHX · Abbreviated 11/08/1999SE
K993171HP Viridia Information System, Models M3150A/ M3151A/ M3153A/ M3154ADSI · Special 10/21/1999SE

Questions and answers

When was Sonos 500 and Sonos 1000 Ultrasound Imaging System cleared by the FDA?

Sonos 500 and Sonos 1000 Ultrasound Imaging System (K905728) received a 510(k) decision of Substantially Equivalent on March 15, 1991, 81 days after the submission was received.

What is the product code of K905728?

The FDA product code is DPT – Probe, Blood-Flow, Extravascular, a Class II (moderate risk) device regulated under 21 CFR 870.2120.