SELICOR, MODELS A100 & D100— 510(k) K020227

Substantially Equivalent

Selicor, Inc.

FDA 510(k) clearance K020227 for SELICOR, MODELS A100 & D100, Substantially Equivalent on 2002-07-30. Applicant: Selicor, Inc.. Device class: 2.

Clearance details

Applicant: Selicor, Inc.
Product code: Code IMJ
Device class: Class 2
Regulation: 21 CFR 890.5290
Advisory panel: Physical Medicine
Date received: 2002-01-22
Decision date: 2002-07-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Antonio, TX, US

Download summary PDF View on FDA.gov ↗

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