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FDA 510(k)

DELTA SCANNER, DELTA SCANNER PRO, DS SPINE PRO, DS SPORTS PRO AND DS REHAB

K-Number: K071878 · 2007-12-07

ApplicantMed-Lectric Corporation
Decision Date2007-12-07
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DELTA SCANNER, DELTA SCANNER PRO, DS SPINE PRO, DS SPORTS PRO AND DS REHAB is the device name listed in this FDA 510(k) record. The listed applicant is Med-Lectric Corporation. It received FDA 510(k) clearance on 2007-12-07 under 510(k) number K071878. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DELTA SCANNER, DELTA SCANNER PRO, DS SPINE PRO, DS SPORTS PRO AND DS REHAB?

DELTA SCANNER, DELTA SCANNER PRO, DS SPINE PRO, DS SPORTS PRO AND DS REHAB is a medical device that received FDA 510(k) clearance on 2007-12-07. The listed applicant is Med-Lectric Corporation. The 510(k) number is K071878.

When did DELTA SCANNER, DELTA SCANNER PRO, DS SPINE PRO, DS SPORTS PRO AND DS REHAB receive FDA 510(k) clearance?

DELTA SCANNER, DELTA SCANNER PRO, DS SPINE PRO, DS SPORTS PRO AND DS REHAB received FDA 510(k) clearance on 2007-12-07, under 510(k) number K071878.

Who is the listed applicant for DELTA SCANNER, DELTA SCANNER PRO, DS SPINE PRO, DS SPORTS PRO AND DS REHAB?

The FDA 510(k) record lists Med-Lectric Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DELTA SCANNER, DELTA SCANNER PRO, DS SPINE PRO, DS SPORTS PRO AND DS REHAB?

The FDA product code for DELTA SCANNER, DELTA SCANNER PRO, DS SPINE PRO, DS SPORTS PRO AND DS REHAB is GZJ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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