HP SONOS 500 AND SONOS 1000 ULTRA. IMAGING SYSTEM— 510(k) K896435

Substantially Equivalent

Hewlett-Packard Co.

FDA 510(k) clearance K896435 for HP SONOS 500 AND SONOS 1000 ULTRA. IMAGING SYSTEM, Substantially Equivalent on 1990-02-07. Applicant: Hewlett-Packard Co.. Device class: 2.

Clearance details

Applicant
Hewlett-Packard Co.
Product code
Code DPT
Device class
Class 2
Regulation
21 CFR 870.2120
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Andover, MA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.