FRYE ADJUSTING INSTRUMENT— 510(k) K021238

Name: FDA 510(k) clearance K021238
Creator: U.S. Food and Drug Administration
Published: 2002-10-09

Substantially Equivalent

Frye Health Systems

FDA 510(k) clearance K021238 for FRYE ADJUSTING INSTRUMENT, Substantially Equivalent on 2002-10-09. Applicant: Frye Health Systems. Device class: Unclassified.

Clearance details

Applicant: Frye Health Systems
Product code: Code LXM
Device class: Unclassified
Advisory panel: Unknown
Date received: 2002-04-18
Decision date: 2002-10-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mesa, AZ, US

Download summary PDF View on FDA.gov ↗

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