ACCUGUIDE MUSCLE INJECTION MONITOR— 510(k) K990793

Name: FDA 510(k) clearance K990793
Creator: U.S. Food and Drug Administration
Published: 1999-10-22

Substantially Equivalent

Medtronic Xomed

FDA 510(k) clearance K990793 for ACCUGUIDE MUSCLE INJECTION MONITOR, Substantially Equivalent on 1999-10-22. Applicant: Medtronic Xomed. Device class: 2.

Clearance details

Applicant: Medtronic Xomed
Product code: Code GXZ
Device class: Class 2
Regulation: 21 CFR 882.1350
Advisory panel: Neurology
Date received: 1999-03-10
Decision date: 1999-10-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

Download summary PDF View on FDA.gov ↗

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