510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K050595Substantially Equivalent

Ft2000 Sequencer for Muscle Stimulator

Midwest Development, Egale WI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K050595 is the FDA 510(k) clearance record for FT2000 SEQUENCER FOR MUSCLE STIMULATOR, a class II device, cleared for Midwest Development on under FDA product code IPF (Stimulator, Muscle, Powered). FDA records list one 510(k) clearance for Midwest Development. As of , FDA records show no recalls naming K050595.

Clearance record

Decision date
Received
(76 days to decision)
Product code
IPF Stimulator, Muscle, Powered
Regulation
21 CFR 890.5850
Device class
Class II
Review panel
Physical Medicine
Applicant
Midwest Development S65w35739 Piper Rd., Egale WI
510(k) summary
Summary PDF
Third party review
No

Clearances, product code IPF

Trailing 12 months
3 clearances under product code IPF in the twelve months to October 2026, June 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code IPF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20262
July 20260
August 20260
September 20260
October 20260