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FDA 510(k)

SONADA ULTRASOUND SYSTEM

K-Number: K993092 · 2000-04-14

ApplicantSonovision Corp.
Decision Date2000-04-14
Product CodeOXO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SONADA ULTRASOUND SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sonovision Corp.. It received FDA 510(k) clearance on 2000-04-14 under 510(k) number K993092. The device is classified under product code OXO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONADA ULTRASOUND SYSTEM?

SONADA ULTRASOUND SYSTEM is a medical device that received FDA 510(k) clearance on 2000-04-14. The listed applicant is Sonovision Corp.. The 510(k) number is K993092.

When did SONADA ULTRASOUND SYSTEM receive FDA 510(k) clearance?

SONADA ULTRASOUND SYSTEM received FDA 510(k) clearance on 2000-04-14, under 510(k) number K993092.

Who is the listed applicant for SONADA ULTRASOUND SYSTEM?

The FDA 510(k) record lists Sonovision Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SONADA ULTRASOUND SYSTEM?

The FDA product code for SONADA ULTRASOUND SYSTEM is OXO.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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