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FDA 510(k)

FT2000 SEQUENCER FOR MUSCLE STIMULATOR

K-Number: K050595 · 2005-05-23

ApplicantMidwest Development
Decision Date2005-05-23
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FT2000 SEQUENCER FOR MUSCLE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Midwest Development. It received FDA 510(k) clearance on 2005-05-23 under 510(k) number K050595. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FT2000 SEQUENCER FOR MUSCLE STIMULATOR?

FT2000 SEQUENCER FOR MUSCLE STIMULATOR is a medical device that received FDA 510(k) clearance on 2005-05-23. The listed applicant is Midwest Development. The 510(k) number is K050595.

When did FT2000 SEQUENCER FOR MUSCLE STIMULATOR receive FDA 510(k) clearance?

FT2000 SEQUENCER FOR MUSCLE STIMULATOR received FDA 510(k) clearance on 2005-05-23, under 510(k) number K050595.

Who is the listed applicant for FT2000 SEQUENCER FOR MUSCLE STIMULATOR?

The FDA 510(k) record lists Midwest Development as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FT2000 SEQUENCER FOR MUSCLE STIMULATOR?

The FDA product code for FT2000 SEQUENCER FOR MUSCLE STIMULATOR 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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