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FDA 510(k)

MICRO-STIM 200

K-Number: K885190 · 1989-04-26

ApplicantTheri-Teck, Inc.
Decision Date1989-04-26
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MICRO-STIM 200 is the device name listed in this FDA 510(k) record. The listed applicant is Theri-Teck, Inc.. It received FDA 510(k) clearance on 1989-04-26 under 510(k) number K885190. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-STIM 200?

MICRO-STIM 200 is a medical device that received FDA 510(k) clearance on 1989-04-26. The listed applicant is Theri-Teck, Inc.. The 510(k) number is K885190.

When did MICRO-STIM 200 receive FDA 510(k) clearance?

MICRO-STIM 200 received FDA 510(k) clearance on 1989-04-26, under 510(k) number K885190.

Who is the listed applicant for MICRO-STIM 200?

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

What is the FDA product code for MICRO-STIM 200?

The FDA product code for MICRO-STIM 200 is GZJ.

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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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