510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K893254Substantially Equivalent

Dynamic System Computerized Podiatric Analyzer

Dalphi, Inc., Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K893254 is the FDA 510(k) clearance record for DYNAMIC SYSTEM COMPUTERIZED PODIATRIC ANALYZER, a class I device, cleared for Dalphi, Inc. on under FDA product code KHX (Platform, Force-Measuring). FDA records list one 510(k) clearance for Dalphi, Inc. As of , FDA records show no recalls naming K893254.

Clearance record

Decision date
Received
(249 days to decision)
Product code
KHX Platform, Force-Measuring
Regulation
21 CFR 890.1575
Device class
Class I
Review panel
Physical Medicine
Applicant
Dalphi, Inc. 1140 19th St. NW, Washington DC
Third party review
No

Clearances, product code KHX

Trailing 12 months

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

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