SPACELINE FEEL 21— 510(k) K953865

Substantially Equivalent

J. Morita USA, Inc.

FDA 510(k) clearance K953865 for SPACELINE FEEL 21, Substantially Equivalent on 1996-03-20. Applicant: J. Morita USA, Inc.. Device class: 1.

Clearance details

Applicant: J. Morita USA, Inc.
Product code: Code EFA
Device class: Class 1
Regulation: 21 CFR 872.4200
Advisory panel: Dental
Date received: 1995-08-17
Decision date: 1996-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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