PATIENT GUIDED KNEE EXERCISER— 510(k) K820120

Name: FDA 510(k) clearance K820120
Creator: U.S. Food and Drug Administration
Published: 1982-01-29

Substantially Equivalent

Richard'S Medical Equip., Inc.

FDA 510(k) clearance K820120 for PATIENT GUIDED KNEE EXERCISER, Substantially Equivalent on 1982-01-29. Applicant: Richard'S Medical Equip., Inc.. Device class: 1.

Clearance details

Applicant: Richard'S Medical Equip., Inc.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1982-01-18
Decision date: 1982-01-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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