POLYMEDIC UPA NERVE STIMULATION NEEDLE; POLYMEDIC UPC NERVE STIMULATION NEEDLE— 510(k) K990100

Name: FDA 510(k) clearance K990100
Creator: U.S. Food and Drug Administration
Published: 2000-08-02

Substantially Equivalent

Te ME NA S.A.R.L.

FDA 510(k) clearance K990100 for POLYMEDIC UPA NERVE STIMULATION NEEDLE; POLYMEDIC UPC NERVE STIMULATION NEEDLE, Substantially Equivalent on 2000-08-02. Applicant: Te ME NA S.A.R.L.. Device class: 2.

Clearance details

Applicant: Te ME NA S.A.R.L.
Product code: Code GXZ
Device class: Class 2
Regulation: 21 CFR 882.1350
Advisory panel: Neurology
Date received: 1999-01-04
Decision date: 2000-08-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oldsmar, FL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.