LACTATE PRO SYSTEM— 510(k) K980908

Substantially Equivalent

Kdk Corp.

FDA 510(k) clearance K980908 for LACTATE PRO SYSTEM, Substantially Equivalent on 1998-09-11. Applicant: Kdk Corp.. Device class: 1.

Clearance details

Applicant: Kdk Corp.
Product code: Code KHP
Device class: Class 1
Regulation: 21 CFR 862.1450
Advisory panel: Clinical Chemistry
Date received: 1998-03-10
Decision date: 1998-09-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kyoto, JP

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.