GRINDGUARD— 510(k) K133037

Name: FDA 510(k) clearance K133037
Creator: U.S. Food and Drug Administration
Published: 2014-01-23

Substantially Equivalent

Grind Guard Technologies, LLC

FDA 510(k) clearance K133037 for GRINDGUARD, Substantially Equivalent on 2014-01-23. Applicant: Grind Guard Technologies, LLC. Device class: Unclassified.

Clearance details

Applicant: Grind Guard Technologies, LLC
Product code: Code OBR
Device class: Unclassified
Advisory panel: Unknown
Date received: 2013-09-26
Decision date: 2014-01-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Leola, PA, US

Download summary PDF View on FDA.gov ↗

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