TUBING, FLEXIBLE, MEDICAL GAS— 510(k) K781416

Name: FDA 510(k) clearance K781416
Creator: U.S. Food and Drug Administration
Published: 1978-09-11

Substantially Equivalent

Vitalab Products Corp.

FDA 510(k) clearance K781416 for TUBING, FLEXIBLE, MEDICAL GAS, Substantially Equivalent on 1978-09-11. Applicant: Vitalab Products Corp.. Device class: 1.

Clearance details

Applicant: Vitalab Products Corp.
Product code: Code BYX
Device class: Class 1
Regulation: 21 CFR 868.5860
Advisory panel: Anesthesiology
Date received: 1978-08-15
Decision date: 1978-09-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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