DeviceClearance

DELTA SCANNER, DELTA SCANNER PRO, DS SPINE PRO, DS SPORTS PRO AND DS REHAB— 510(k) K071878

Substantially Equivalent

Med-Lectric Corporation

FDA 510(k) clearance K071878 for DELTA SCANNER, DELTA SCANNER PRO, DS SPINE PRO, DS SPORTS PRO AND DS REHAB, Substantially Equivalent on 2007-12-07. Applicant: Med-Lectric Corporation.

Clearance details

Applicant
Med-Lectric Corporation
Product code
Code GZJ
Advisory panel
Neurology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Kemah, TX, US
Download summary PDFView on FDA.gov ↗

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