KRONAMAX HUMAN PERFORMANCE LAB— 510(k) K902219

Name: FDA 510(k) clearance K902219
Creator: U.S. Food and Drug Administration
Published: 1990-07-25

Substantially Equivalent

Physicians Digital Co.

FDA 510(k) clearance K902219 for KRONAMAX HUMAN PERFORMANCE LAB, Substantially Equivalent on 1990-07-25. Applicant: Physicians Digital Co.. Device class: 2.

Clearance details

Applicant: Physicians Digital Co.
Product code: Code IKK
Device class: Class 2
Regulation: 21 CFR 890.1925
Advisory panel: Physical Medicine
Date received: 1990-05-16
Decision date: 1990-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Richmond, CA, US

Download summary PDF View on FDA.gov ↗

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