510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K980908Substantially Equivalent

Lactate Pro System

Kdk Corp., Kyoto, JP / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K980908 is the FDA 510(k) clearance record for LACTATE PRO SYSTEM, a class I device, cleared for Kdk Corp. on under FDA product code KHP (Acid, Lactic, Enzymatic Method). FDA records list one 510(k) clearance for Kdk Corp. As of , FDA records show no recalls naming K980908.

Clearance record

Decision date
Received
(185 days to decision)
Product code
KHP Acid, Lactic, Enzymatic Method
Regulation
21 CFR 862.1450
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Kdk Corp. 57 Nishiaketa-Cho,, Kyoto, JP
510(k) summary
Summary
Third party review
No

Clearances, product code KHP

Trailing 12 months

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

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