RAPIDEX BIOLOGICAL SURFACTANT— 510(k) K862282

Name: FDA 510(k) clearance K862282
Creator: U.S. Food and Drug Administration
Published: 1987-05-11

Substantially Equivalent

Rapidex of London

FDA 510(k) clearance K862282 for RAPIDEX BIOLOGICAL SURFACTANT, Substantially Equivalent on 1987-05-11. Applicant: Rapidex of London. Device class: 1.

Clearance details

Applicant: Rapidex of London
Product code: Code FLG
Device class: Class 1
Regulation: 21 CFR 880.6150
Advisory panel: General Hospital
Date received: 1986-06-16
Decision date: 1987-05-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Richmond, Surrey, GB

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