BOTTLE BREATHING DEVICE— 510(k) K780558

Name: FDA 510(k) clearance K780558
Creator: U.S. Food and Drug Administration
Published: 1978-05-26

Substantially Equivalent

B & F Medical Products, Inc.

FDA 510(k) clearance K780558 for BOTTLE BREATHING DEVICE, Substantially Equivalent on 1978-05-26. Applicant: B & F Medical Products, Inc.. Device class: 1.

Clearance details

Applicant: B & F Medical Products, Inc.
Product code: Code BYO
Device class: Class 1
Regulation: 21 CFR 868.5220
Advisory panel: Anesthesiology
Date received: 1978-04-05
Decision date: 1978-05-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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