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FDA 510(k)

LED STIMULATOR LS-05

K-Number: K834442 · 1984-08-08

ApplicantTeca, Inc.
Decision Date1984-08-08
Product CodeGWE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

LED STIMULATOR LS-05 is the device name listed in this FDA 510(k) record. The listed applicant is Teca, Inc.. It received FDA 510(k) clearance on 1984-08-08 under 510(k) number K834442. The device is classified under product code GWE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LED STIMULATOR LS-05?

LED STIMULATOR LS-05 is a medical device that received FDA 510(k) clearance on 1984-08-08. The listed applicant is Teca, Inc.. The 510(k) number is K834442.

When did LED STIMULATOR LS-05 receive FDA 510(k) clearance?

LED STIMULATOR LS-05 received FDA 510(k) clearance on 1984-08-08, under 510(k) number K834442.

Who is the listed applicant for LED STIMULATOR LS-05?

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 LED STIMULATOR LS-05?

The FDA product code for LED STIMULATOR LS-05 is GWE.

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Related Devices (Code: GWE)

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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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