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FDA 510(k)

TECA VISUAL/AUDIO STIMULATOR MODEL CS-2

K-Number: K813009 · 1981-12-14

ApplicantTeca, Inc.
Decision Date1981-12-14
Product CodeGWJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TECA VISUAL/AUDIO STIMULATOR MODEL CS-2 is the device name listed in this FDA 510(k) record. The listed applicant is Teca, Inc.. It received FDA 510(k) clearance on 1981-12-14 under 510(k) number K813009. The device is classified under product code GWJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECA VISUAL/AUDIO STIMULATOR MODEL CS-2?

TECA VISUAL/AUDIO STIMULATOR MODEL CS-2 is a medical device that received FDA 510(k) clearance on 1981-12-14. The listed applicant is Teca, Inc.. The 510(k) number is K813009.

When did TECA VISUAL/AUDIO STIMULATOR MODEL CS-2 receive FDA 510(k) clearance?

TECA VISUAL/AUDIO STIMULATOR MODEL CS-2 received FDA 510(k) clearance on 1981-12-14, under 510(k) number K813009.

Who is the listed applicant for TECA VISUAL/AUDIO STIMULATOR MODEL CS-2?

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

What is the FDA product code for TECA VISUAL/AUDIO STIMULATOR MODEL CS-2?

The FDA product code for TECA VISUAL/AUDIO STIMULATOR MODEL CS-2 is GWJ.

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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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