510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K901566Substantially Equivalent

Promatron 3000

Promatek Medical Systems, Inc., Joliet IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K901566 is the FDA 510(k) clearance record for PROMATRON 3000, a class II device, cleared for Promatek Medical Systems, Inc. on under FDA product code IKK (System, Isokinetic Testing And Evaluation). FDA records list one 510(k) clearance for Promatek Medical Systems, Inc. As of , FDA records show no recalls naming K901566.

Clearance record

Decision date
Received
(209 days to decision)
Product code
IKK System, Isokinetic Testing And Evaluation
Regulation
21 CFR 890.1925
Device class
Class II
Review panel
Physical Medicine
Applicant
Promatek Medical Systems, Inc. 1851 Black Rd., Joliet IL
Third party review
No

Clearances, product code IKK

Trailing 12 months

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

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