SILICONE RUBBER-BI NASOPHARYNGEAL AIR— 510(k) K792018

Name: FDA 510(k) clearance K792018
Creator: U.S. Food and Drug Administration
Published: 1979-11-13

Substantially Equivalent

Vesta, Inc.

FDA 510(k) clearance K792018 for SILICONE RUBBER-BI NASOPHARYNGEAL AIR, Substantially Equivalent on 1979-11-13. Applicant: Vesta, Inc.. Device class: 1.

Clearance details

Applicant: Vesta, Inc.
Product code: Code BTQ
Device class: Class 1
Regulation: 21 CFR 868.5100
Advisory panel: Anesthesiology
Date received: 1979-10-09
Decision date: 1979-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K903618 — ROBERTAZZI NASOPHARYNGEAL AIRWAY1991-01-08
K900456 — POLAMEDCO NASOPAHARYNGEAL AIRWAY1990-04-19

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K792719 — 3 WAY URETHRAL IRRIGATION CATHETER1980-01-16

Data sourced from openFDA. This site is unofficial and independent of the FDA.