VYGON GUEDEL AIRWAY 511 VYGON BERMANN/OROPHAR AIRW— 510(k) K851480

Name: FDA 510(k) clearance K851480
Creator: U.S. Food and Drug Administration
Published: 1985-05-07

Substantially Equivalent

Vygon Corp.

FDA 510(k) clearance K851480 for VYGON GUEDEL AIRWAY 511 VYGON BERMANN/OROPHAR AIRW, Substantially Equivalent on 1985-05-07. Applicant: Vygon Corp.. Device class: 2.

Clearance details

Applicant: Vygon Corp.
Product code: Code LAE
Device class: Class 2
Regulation: 21 CFR 862.3270
Advisory panel: Clinical Toxicology
Date received: 1985-04-15
Decision date: 1985-05-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: East Rutherford, NJ, US

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