REGNELL HYDRAULIC FEMORAL PROTHESIS— 510(k) K830285

Name: FDA 510(k) clearance K830285
Creator: U.S. Food and Drug Administration
Published: 1983-03-09

Substantially Equivalent

Besco Financial Service

FDA 510(k) clearance K830285 for REGNELL HYDRAULIC FEMORAL PROTHESIS, Substantially Equivalent on 1983-03-09. Applicant: Besco Financial Service. Device class: 2.

Clearance details

Applicant: Besco Financial Service
Product code: Code KFX
Device class: Class 2
Regulation: 21 CFR 890.3500
Advisory panel: Physical Medicine
Date received: 1983-01-27
Decision date: 1983-03-09
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.