510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K883462Substantially Equivalent

If-II (Tm), Model 9800

Medical Devices Inc., St. Paul MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K883462 is the FDA 510(k) clearance record for IF-II (TM), MODEL 9800, a class II device, cleared for Medical Devices, Inc. on under FDA product code LIH (Interferential Current Therapy). FDA records list 49 510(k) clearances for Medical Devices, Inc., from to . As of , FDA records show no recalls naming K883462.

Clearance record

Decision date
Received
(282 days to decision)
Product code
LIH Interferential Current Therapy
Regulation
21 CFR 882.5890
Device class
Class II
Review panel
Neurology
Applicant
Medical Devices, Inc. 833 Third St. Southwest, St. Paul MN
Third party review
No

Clearances, product code LIH

Trailing 12 months

FDA records hold no clearances under product code LIH in the trailing twelve months.

FDA records show no clearances under product code LIH in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LIH, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260