VENTURI MASK/DELIVERY SYSTEM #'S— 510(k) K810373

Name: FDA 510(k) clearance K810373
Creator: U.S. Food and Drug Administration
Published: 1981-03-17

Substantially Equivalent

Todd Industries, Inc.

FDA 510(k) clearance K810373 for VENTURI MASK/DELIVERY SYSTEM #'S, Substantially Equivalent on 1981-03-17. Applicant: Todd Industries, Inc.. Device class: 1.

Clearance details

Applicant: Todd Industries, Inc.
Product code: Code BYF
Device class: Class 1
Regulation: 21 CFR 868.5600
Advisory panel: Anesthesiology
Date received: 1981-02-12
Decision date: 1981-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K810339 — NOSECLIP #61181981-03-17
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K810341 — LIFELINE IPPB SET-UP1981-03-17
K810342 — NASAL CANNULA1981-03-17
K810343 — NEBULIZERS1981-03-17

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