510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K902219Substantially Equivalent

Kronamax Human Performance Lab

Physicians Digital Co., Richmond CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902219 is the FDA 510(k) clearance record for KRONAMAX HUMAN PERFORMANCE LAB, a class II device, cleared for Physicians Digital Co. on under FDA product code IKK (System, Isokinetic Testing And Evaluation). FDA records list 2 510(k) clearances for Physicians Digital Co., from to . As of , FDA records show no recalls naming K902219.

Clearance record

Decision date
Received
(70 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
Physicians Digital Co. 12600 San Pablo Ave., Richmond CA
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