MAX ADJUSTING INSTRUMENT— 510(k) K082218

Name: FDA 510(k) clearance K082218
Creator: U.S. Food and Drug Administration
Published: 2008-08-13

Substantially Equivalent

Manna Omni International, Inc.

FDA 510(k) clearance K082218 for MAX ADJUSTING INSTRUMENT, Substantially Equivalent on 2008-08-13. Applicant: Manna Omni International, Inc.. Device class: Unclassified.

Clearance details

Applicant: Manna Omni International, Inc.
Product code: Code LXM
Device class: Unclassified
Advisory panel: Unknown
Date received: 2008-08-06
Decision date: 2008-08-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fullerton, CA, US

Download summary PDF View on FDA.gov ↗

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