MODIFIED SYST: SONOS 500/1000 ULTRSOUND IMAG SYST— 510(k) K904832

Name: FDA 510(k) clearance K904832
Creator: U.S. Food and Drug Administration
Published: 1991-04-22

Substantially Equivalent

Hewlett-Packard Co.

FDA 510(k) clearance K904832 for MODIFIED SYST: SONOS 500/1000 ULTRSOUND IMAG SYST, Substantially Equivalent on 1991-04-22. Applicant: Hewlett-Packard Co.. Device class: 2.

Clearance details

Applicant: Hewlett-Packard Co.
Product code: Code DXK
Device class: Class 2
Regulation: 21 CFR 870.2330
Advisory panel: Cardiovascular
Date received: 1990-10-23
Decision date: 1991-04-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Andover, MA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.