KRONAMAX KUBE— 510(k) K893903

Substantially Equivalent

Physicians Digital Co.

FDA 510(k) clearance K893903 for KRONAMAX KUBE, Substantially Equivalent on 1989-11-29. Applicant: Physicians Digital Co.. Device class: 1.

Clearance details

Applicant: Physicians Digital Co.
Product code: Code KQX
Device class: Class 1
Regulation: 21 CFR 888.1500
Advisory panel: Orthopedic
Date received: 1989-05-30
Decision date: 1989-11-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Richmond, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Physicians Digital Co.

K902219 — KRONAMAX HUMAN PERFORMANCE LAB1990-07-25

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