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FDA 510(k)

TEC-SON II

K-Number: K820162 · 1982-02-24

ApplicantCalifornia Technics, Inc.
Decision Date1982-02-24
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TEC-SON II 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 1982-02-24 under 510(k) number K820162. 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 TEC-SON II?

TEC-SON II is a medical device that received FDA 510(k) clearance on 1982-02-24. The listed applicant is California Technics, Inc.. The 510(k) number is K820162.

When did TEC-SON II receive FDA 510(k) clearance?

TEC-SON II received FDA 510(k) clearance on 1982-02-24, under 510(k) number K820162.

Who is the listed applicant for TEC-SON II?

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 TEC-SON II?

The FDA product code for TEC-SON II is ELC.

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 UNITK811396SONUS V

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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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