PULMO-SONIC— 510(k) K781073

Substantially Equivalent

The Devilbiss Co.

FDA 510(k) clearance K781073 for PULMO-SONIC, Substantially Equivalent on 1978-09-27. Applicant: The Devilbiss Co.. Device class: 1.

Clearance details

Applicant: The Devilbiss Co.
Product code: Code CCQ
Device class: Class 1
Regulation: 21 CFR 868.5640
Advisory panel: Anesthesiology
Date received: 1978-06-26
Decision date: 1978-09-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from The Devilbiss Co.

K874041 — DEVILBISS MODEL 8500D1987-12-23
K872094 — VACU-AIDE1987-10-15
K872826 — ULTRA-NEB 99 ULTRASONIC NEBULIZER1987-09-04
K872470 — DEVO/MC44 OXYGEN CONCENTRATOR1987-08-03
K854520 — PULMO-AIDE MODEL 5610D1985-12-09

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