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FDA 510(k)

SONUS V

K-Number: K811396 · 1981-06-26

ApplicantCalifornia Technics, Inc.
Decision Date1981-06-26
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SONUS V is the device name listed in this FDA 510(k) record. The listed applicant is California Technics, Inc.. It received FDA 510(k) clearance on 1981-06-26 under 510(k) number K811396. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONUS V?

SONUS V is a medical device that received FDA 510(k) clearance on 1981-06-26. The listed applicant is California Technics, Inc.. The 510(k) number is K811396.

When did SONUS V receive FDA 510(k) clearance?

SONUS V received FDA 510(k) clearance on 1981-06-26, under 510(k) number K811396.

Who is the listed applicant for SONUS V?

The FDA 510(k) record lists California Technics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SONUS V?

The FDA product code for SONUS V is ELC.

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.

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Other records listing California Technics, Inc. 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.

K832443ULTRASONIC DENTAL PROPHYLAXIS UNITK820162TEC-SON II

Related Devices (Code: ELC)

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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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