VOL. VENTILATOR SETUP W/OUT NEBULIZER— 510(k) K772069

Name: FDA 510(k) clearance K772069
Creator: U.S. Food and Drug Administration
Published: 1977-11-15

Substantially Equivalent

Inspiron Corp.

FDA 510(k) clearance K772069 for VOL. VENTILATOR SETUP W/OUT NEBULIZER, Substantially Equivalent on 1977-11-15. Applicant: Inspiron Corp.. Device class: 1.

Clearance details

Applicant: Inspiron Corp.
Product code: Code BZO
Device class: Class 1
Regulation: 21 CFR 868.5975
Advisory panel: Anesthesiology
Date received: 1977-11-01
Decision date: 1977-11-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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K953784 — UNICOR, INC. CORRUGATED TUBING1995-09-19
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K952011 — PRIMA BREATHING BAGS1995-05-22
K952012 — PRIMA CUSTOM ANESTESIA CIRCUIT1995-05-22

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K840935 — MANUAL RESUSCITATION SYSTEM1984-04-05
K841158 — NEBULO 28 NEBULIZER KIT1984-03-30

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