THE BRIGHT MEDICAL DILATION RETRACTOR SYSTEM— 510(k) K992898

Name: FDA 510(k) clearance K992898
Creator: U.S. Food and Drug Administration
Published: 1999-10-21

Substantially Equivalent

Bright Medical Instruments

FDA 510(k) clearance K992898 for THE BRIGHT MEDICAL DILATION RETRACTOR SYSTEM, Substantially Equivalent on 1999-10-21. Applicant: Bright Medical Instruments. Device class: 2.

Clearance details

Applicant: Bright Medical Instruments
Product code: Code GZT
Device class: Class 2
Regulation: 21 CFR 882.4800
Advisory panel: Neurology
Date received: 1999-08-27
Decision date: 1999-10-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boca Raton, 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.