MANIFOLD/NEBULIZER BREATHING PRODUCTS— 510(k) K791469

Name: FDA 510(k) clearance K791469
Creator: U.S. Food and Drug Administration
Published: 1979-08-28

Substantially Equivalent

Hospitak, Inc.

FDA 510(k) clearance K791469 for MANIFOLD/NEBULIZER BREATHING PRODUCTS, Substantially Equivalent on 1979-08-28. Applicant: Hospitak, Inc.. Device class: 1.

Clearance details

Applicant: Hospitak, Inc.
Product code: Code BZO
Device class: Class 1
Regulation: 21 CFR 868.5975
Advisory panel: Anesthesiology
Date received: 1979-08-06
Decision date: 1979-08-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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