FITKIT I CHECKUP KIT— 510(k) K830340

Substantially Equivalent

Boditestor

FDA 510(k) clearance K830340 for FITKIT I CHECKUP KIT, Substantially Equivalent on 1983-08-16. Applicant: Boditestor. Device class: 1.

Clearance details

Applicant: Boditestor
Product code: Code CDM
Device class: Class 1
Regulation: 21 CFR 862.1785
Advisory panel: Clinical Chemistry
Date received: 1983-02-02
Decision date: 1983-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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