FT2000 SEQUENCER FOR MUSCLE STIMULATOR— 510(k) K050595

Substantially Equivalent

Midwest Development

FDA 510(k) clearance K050595 for FT2000 SEQUENCER FOR MUSCLE STIMULATOR, Substantially Equivalent on 2005-05-23. Applicant: Midwest Development.

Clearance details

Applicant
Midwest Development
Product code
Code IPF
Advisory panel
Physical Medicine
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Egale, WI, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.