510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K050847Substantially Equivalent

If True Sine Interferential Stimulator, Model Wl-2206A

Theratech, Inc., Madison TN / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K050847 is the FDA 510(k) clearance record for IF TRUE SINE INTERFERENTIAL STIMULATOR, MODEL WL-2206A, a class II device, cleared for Theratech, Inc. on under FDA product code IPF (Stimulator, Muscle, Powered). FDA records list 5 510(k) clearances for Theratech, Inc., from to . As of , FDA records show no recalls naming K050847.

Clearance record

Decision date
Received
(74 days to decision)
Product code
IPF Stimulator, Muscle, Powered
Regulation
21 CFR 890.5850
Device class
Class II
Review panel
Physical Medicine
Applicant
Theratech, Inc. 1109 Myatt Blvd., Madison TN
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