MODEL K210 AND K211 FLUIDOTHERAPY UNITS— 510(k) K871802

Name: FDA 510(k) clearance K871802
Creator: U.S. Food and Drug Administration
Published: 1987-09-04

Substantially Equivalent

Henley Intl.

FDA 510(k) clearance K871802 for MODEL K210 AND K211 FLUIDOTHERAPY UNITS, Substantially Equivalent on 1987-09-04. Applicant: Henley Intl.. Device class: 2.

Clearance details

Applicant: Henley Intl.
Product code: Code LSB
Device class: Class 2
Regulation: 21 CFR 890.5100
Advisory panel: Physical Medicine
Date received: 1987-05-08
Decision date: 1987-09-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

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