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FDA 510(k)

STIMUTRON MODEL 100

K-Number: K865054 · 1987-02-26

ApplicantThe Austin-Lenick Co.
Decision Date1987-02-26
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

STIMUTRON MODEL 100 is the device name listed in this FDA 510(k) record. The listed applicant is The Austin-Lenick Co.. It received FDA 510(k) clearance on 1987-02-26 under 510(k) number K865054. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the STIMUTRON MODEL 100?

STIMUTRON MODEL 100 is a medical device that received FDA 510(k) clearance on 1987-02-26. The listed applicant is The Austin-Lenick Co.. The 510(k) number is K865054.

When did STIMUTRON MODEL 100 receive FDA 510(k) clearance?

STIMUTRON MODEL 100 received FDA 510(k) clearance on 1987-02-26, under 510(k) number K865054.

Who is the listed applicant for STIMUTRON MODEL 100?

The FDA 510(k) record lists The Austin-Lenick Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STIMUTRON MODEL 100?

The FDA product code for STIMUTRON MODEL 100 is IPF.

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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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