HP SONOS 500 AND SONOS 1000 ULTRA. IMAGING SYSTEM
K-Number: K896435 · 1990-02-07
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Device Summary
Frequently Asked Questions
What is the HP SONOS 500 AND SONOS 1000 ULTRA. IMAGING SYSTEM?
HP SONOS 500 AND SONOS 1000 ULTRA. IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1990-02-07. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K896435.
When did HP SONOS 500 AND SONOS 1000 ULTRA. IMAGING SYSTEM receive FDA 510(k) clearance?
HP SONOS 500 AND SONOS 1000 ULTRA. IMAGING SYSTEM received FDA 510(k) clearance on 1990-02-07, under 510(k) number K896435.
Who is the listed applicant for HP SONOS 500 AND SONOS 1000 ULTRA. IMAGING SYSTEM?
The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HP SONOS 500 AND SONOS 1000 ULTRA. IMAGING SYSTEM?
The FDA product code for HP SONOS 500 AND SONOS 1000 ULTRA. IMAGING SYSTEM is DPT.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Hewlett-Packard Co. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: DPT)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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