KINETIC 8080 HAND & WRIST CONTIN. PASSIVE MACHINE— 510(k) K850332

Name: FDA 510(k) clearance K850332
Creator: U.S. Food and Drug Administration
Published: 1985-05-01

Substantially Equivalent

Richards Medical Co., Inc.

FDA 510(k) clearance K850332 for KINETIC 8080 HAND & WRIST CONTIN. PASSIVE MACHINE, Substantially Equivalent on 1985-05-01. Applicant: Richards Medical Co., Inc.. Device class: 1.

Clearance details

Applicant: Richards Medical Co., Inc.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1985-01-28
Decision date: 1985-05-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Memphis, TN, US

Download summary PDF View on FDA.gov ↗

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