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FDA 510(k)

SONOS 100 ULTRASOUND IMAGING SYSTEM

K-Number: K921036 · 1992-05-29

ApplicantHewlett-Packard Co.
Decision Date1992-05-29
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SONOS 100 ULTRASOUND IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1992-05-29 under 510(k) number K921036. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONOS 100 ULTRASOUND IMAGING SYSTEM?

SONOS 100 ULTRASOUND IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1992-05-29. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K921036.

When did SONOS 100 ULTRASOUND IMAGING SYSTEM receive FDA 510(k) clearance?

SONOS 100 ULTRASOUND IMAGING SYSTEM received FDA 510(k) clearance on 1992-05-29, under 510(k) number K921036.

Who is the listed applicant for SONOS 100 ULTRASOUND 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 SONOS 100 ULTRASOUND IMAGING SYSTEM?

The FDA product code for SONOS 100 ULTRASOUND IMAGING SYSTEM is ITX.

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Related Devices (Code: ITX)

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.

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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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