I.P.P.B., DIS. W/MANIFOLD/NEBULIZER— 510(k) K760221

Name: FDA 510(k) clearance K760221
Creator: U.S. Food and Drug Administration
Published: 1976-08-03

Substantially Equivalent

Manner Medical Products

FDA 510(k) clearance K760221 for I.P.P.B., DIS. W/MANIFOLD/NEBULIZER, Substantially Equivalent on 1976-08-03. Applicant: Manner Medical Products. Device class: 2.

Clearance details

Applicant: Manner Medical Products
Product code: Code CBO
Device class: Class 2
Regulation: 21 CFR 868.5955
Advisory panel: Anesthesiology
Date received: 1976-07-12
Decision date: 1976-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K791904 — IMV W/BAG & HOSES #M-5091979-10-09
K791905 — IMV W/BAG & TUBING #M-5081979-10-09
K791906 — IMV W/BAG #M-5071979-10-09

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K760218 — CANNULAE, PLASTIC DISPOSABLE NASAL1976-08-03
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K760220 — TUBING, SINGLE USE OXYGEN SUPPLY1976-08-03

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