RESPIRATOR/GILL 1/SIMV— 510(k) K781706

Name: FDA 510(k) clearance K781706
Creator: U.S. Food and Drug Administration
Published: 1979-01-22

Substantially Equivalent

Chemetron Medical Products, Inc.

FDA 510(k) clearance K781706 for RESPIRATOR/GILL 1/SIMV, Substantially Equivalent on 1979-01-22. Applicant: Chemetron Medical Products, Inc.. Device class: 2.

Clearance details

Applicant: Chemetron Medical Products, Inc.
Product code: Code CBO
Device class: Class 2
Regulation: 21 CFR 868.5955
Advisory panel: Anesthesiology
Date received: 1978-10-10
Decision date: 1979-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K811991 — SIMVAC1981-08-12
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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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K781537 — NEBULIZER/HUMIDIFIER1978-10-10
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K781541 — FLOMETER1978-09-26

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