510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K770417Substantially Equivalent

Animator

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

K770417 is the FDA 510(k) clearance record for ANIMATOR, a class I device, cleared for Kdk Medical Products on under FDA product code ITJ (Walker, Mechanical). FDA records list one 510(k) clearance for Kdk Medical Products. As of , FDA records show no recalls naming K770417.

Clearance record

Decision date
Received
(42 days to decision)
Product code
ITJ Walker, Mechanical
Regulation
21 CFR 890.3825
Device class
Class I
Review panel
Physical Medicine
Applicant
Kdk Medical Products 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code ITJ

Trailing 12 months

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

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