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FDA 510(k)

#ST10 PROGR. EVOKED RESPONSE STIMULATOR

K-Number: K822744 · 1982-11-03

ApplicantTeca, Inc.
Decision Date1982-11-03
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

#ST10 PROGR. EVOKED RESPONSE 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 1982-11-03 under 510(k) number K822744. The device is classified under product code GWF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the #ST10 PROGR. EVOKED RESPONSE STIMULATOR?

#ST10 PROGR. EVOKED RESPONSE STIMULATOR is a medical device that received FDA 510(k) clearance on 1982-11-03. The listed applicant is Teca, Inc.. The 510(k) number is K822744.

When did #ST10 PROGR. EVOKED RESPONSE STIMULATOR receive FDA 510(k) clearance?

#ST10 PROGR. EVOKED RESPONSE STIMULATOR received FDA 510(k) clearance on 1982-11-03, under 510(k) number K822744.

Who is the listed applicant for #ST10 PROGR. EVOKED RESPONSE 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 #ST10 PROGR. EVOKED RESPONSE STIMULATOR?

The FDA product code for #ST10 PROGR. EVOKED RESPONSE STIMULATOR is GWF.

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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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