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FDA 510(k)

TECA NEUROPTO WITH OS-5 STIMULATOR

K-Number: K861069 · 1987-01-27

ApplicantTeca, Inc.
Decision Date1987-01-27
Product CodeGWE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TECA NEUROPTO WITH OS-5 STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Teca, Inc.. It received FDA 510(k) clearance on 1987-01-27 under 510(k) number K861069. 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 TECA NEUROPTO WITH OS-5 STIMULATOR?

TECA NEUROPTO WITH OS-5 STIMULATOR is a medical device that received FDA 510(k) clearance on 1987-01-27. The listed applicant is Teca, Inc.. The 510(k) number is K861069.

When did TECA NEUROPTO WITH OS-5 STIMULATOR receive FDA 510(k) clearance?

TECA NEUROPTO WITH OS-5 STIMULATOR received FDA 510(k) clearance on 1987-01-27, under 510(k) number K861069.

Who is the listed applicant for TECA NEUROPTO WITH OS-5 STIMULATOR?

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 NEUROPTO WITH OS-5 STIMULATOR?

The FDA product code for TECA NEUROPTO WITH OS-5 STIMULATOR is GWE.

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Other records listing Teca, Inc. as applicant

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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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