SPIROMETER, INCENTIVE CATALOG # 1750— 510(k) K781831

Name: FDA 510(k) clearance K781831
Creator: U.S. Food and Drug Administration
Published: 1978-12-15

Substantially Equivalent

Hudson Oxygen Therapy Sales Co.

FDA 510(k) clearance K781831 for SPIROMETER, INCENTIVE CATALOG # 1750, Substantially Equivalent on 1978-12-15. Applicant: Hudson Oxygen Therapy Sales Co.. Device class: 2.

Clearance details

Applicant: Hudson Oxygen Therapy Sales Co.
Product code: Code BWF
Device class: Class 2
Regulation: 21 CFR 868.5690
Advisory panel: Anesthesiology
Date received: 1978-10-30
Decision date: 1978-12-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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