AVID-NIT CERVICAL REGIONAL ANESTHESIA NEEDLE— 510(k) K000117

Name: FDA 510(k) clearance K000117
Creator: U.S. Food and Drug Administration
Published: 2000-04-13

Substantially Equivalent

Avid Medical, Inc.

FDA 510(k) clearance K000117 for AVID-NIT CERVICAL REGIONAL ANESTHESIA NEEDLE, Substantially Equivalent on 2000-04-13. Applicant: Avid Medical, Inc.. Device class: 2.

Clearance details

Applicant: Avid Medical, Inc.
Product code: Code HEE
Device class: Class 2
Regulation: 21 CFR 884.5100
Advisory panel: Obstetrics/Gynecology
Date received: 2000-01-14
Decision date: 2000-04-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Toano, VA, US

Download summary PDF View on FDA.gov ↗

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