SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODES— 510(k) K953242

Name: FDA 510(k) clearance K953242
Creator: U.S. Food and Drug Administration
Published: 1995-10-06

Substantially Equivalent

Symbiosis Corp.

FDA 510(k) clearance K953242 for SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODES, Substantially Equivalent on 1995-10-06. Applicant: Symbiosis Corp.. Device class: 2.

Clearance details

Applicant: Symbiosis Corp.
Product code: Product code KNF
Device class: Class 2
Regulation: 21 CFR 884.4160
Advisory panel: Obstetrics/Gynecology
Date received: 1995-07-11
Decision date: 1995-10-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

Download summary PDF View on FDA.gov ↗

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