510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K820784Substantially Equivalent

Clinic 2000 Model Multi-Frecodyn Device

Dimeco, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K820784 is the FDA 510(k) clearance record for CLINIC 2000 MODEL MULTI-FRECODYN DEVICE, a class II device, cleared for Dimeco on under FDA product code IPF (Stimulator, Muscle, Powered). FDA records list one 510(k) clearance for Dimeco. As of , FDA records show no recalls naming K820784.

Clearance record

Decision date
Received
(30 days to decision)
Product code
IPF Stimulator, Muscle, Powered
Regulation
21 CFR 890.5850
Device class
Class II
Review panel
Physical Medicine
Applicant
Dimeco 803 N. Front St. Suite 3, Mchenry IL
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