VAPORTRODE VAPORIZATION ELECTRODE -GROOVED/FLUTED/SPIKED(GVE-B,GVE-F,GVE-S) & VAPORTOMME VAPORIZATION LOOP (GVE-LG)— 510(k) K964594

Name: FDA 510(k) clearance K964594
Creator: U.S. Food and Drug Administration
Published: 1997-08-15

Substantially Equivalent

Circon Corp.

FDA 510(k) clearance K964594 for VAPORTRODE VAPORIZATION ELECTRODE -GROOVED/FLUTED/SPIKED(GVE-B,GVE-F,GVE-S) & VAPORTOMME VAPORIZATION LOOP (GVE-LG), Substantially Equivalent on 1997-08-15. Applicant: Circon Corp.. Device class: 2.

Clearance details

Applicant: Circon Corp.
Product code: Product code KNF
Device class: Class 2
Regulation: 21 CFR 884.4160
Advisory panel: Obstetrics/Gynecology
Date received: 1996-11-15
Decision date: 1997-08-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stamford, CT, US

Download summary PDF View on FDA.gov ↗

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