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FDA 510(k)

VERIZON WIRELESS REMOTE HEALTH MANAGEMENT SYSTEM

K-Number: K122458 · 2013-07-30

ApplicantCello Partnership D/B/A Verizon Wireless
Decision Date2013-07-30
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VERIZON WIRELESS REMOTE HEALTH MANAGEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cello Partnership D/B/A Verizon Wireless. It received FDA 510(k) clearance on 2013-07-30 under 510(k) number K122458. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERIZON WIRELESS REMOTE HEALTH MANAGEMENT SYSTEM?

VERIZON WIRELESS REMOTE HEALTH MANAGEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 2013-07-30. The listed applicant is Cello Partnership D/B/A Verizon Wireless. The 510(k) number is K122458.

When did VERIZON WIRELESS REMOTE HEALTH MANAGEMENT SYSTEM receive FDA 510(k) clearance?

VERIZON WIRELESS REMOTE HEALTH MANAGEMENT SYSTEM received FDA 510(k) clearance on 2013-07-30, under 510(k) number K122458.

Who is the listed applicant for VERIZON WIRELESS REMOTE HEALTH MANAGEMENT SYSTEM?

The FDA 510(k) record lists Cello Partnership D/B/A Verizon Wireless as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VERIZON WIRELESS REMOTE HEALTH MANAGEMENT SYSTEM?

The FDA product code for VERIZON WIRELESS REMOTE HEALTH MANAGEMENT SYSTEM is DRG.

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Related Devices (Code: DRG)

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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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