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FDA 510(k)

WELLNESSPRO 2010

K-Number: K062616 · 2007-07-06

Decision Date2007-07-06
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

WELLNESSPRO 2010 is the device name listed in this FDA 510(k) record. The listed applicant is Intelsource Group, Inc.. It received FDA 510(k) clearance on 2007-07-06 under 510(k) number K062616. 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 WELLNESSPRO 2010?

WELLNESSPRO 2010 is a medical device that received FDA 510(k) clearance on 2007-07-06. The listed applicant is Intelsource Group, Inc.. The 510(k) number is K062616.

When did WELLNESSPRO 2010 receive FDA 510(k) clearance?

WELLNESSPRO 2010 received FDA 510(k) clearance on 2007-07-06, under 510(k) number K062616.

Who is the listed applicant for WELLNESSPRO 2010?

The FDA 510(k) record lists Intelsource Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WELLNESSPRO 2010?

The FDA product code for WELLNESSPRO 2010 is GZJ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: GZJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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