510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K821903Substantially Equivalent

Disc-O-Aid

M. Dahm International ApS, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K821903 is the FDA 510(k) clearance record for DISC-O-AID, a class I device, cleared for M. Dahm International Aps on under FDA product code IKX (Aid, Transfer). FDA records list one 510(k) clearance for M. Dahm International Aps. As of , FDA records show no recalls naming K821903.

Clearance record

Decision date
Received
(22 days to decision)
Product code
IKX Aid, Transfer
Regulation
21 CFR 890.5050
Device class
Class I
Review panel
Physical Medicine
Applicant
M. Dahm International Aps 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code IKX

Trailing 12 months

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

FDA records show no clearances under product code IKX in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code IKX, 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