VERIZON WIRELESS REMOTE HEALTH MANAGEMENT SYSTEM— 510(k) K122458

Substantially Equivalent

Cello Partnership D/B/A Verizon Wireless

FDA 510(k) clearance K122458 for VERIZON WIRELESS REMOTE HEALTH MANAGEMENT SYSTEM, Substantially Equivalent on 2013-07-30. Applicant: Cello Partnership D/B/A Verizon Wireless.

Clearance details

Applicant
Cello Partnership D/B/A Verizon Wireless
Product code
Code DRG
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Washington, DC, US
Download summary PDFView on FDA.gov ↗

Adverse events under product code DRG

product code DRG
Death
5
Total
5

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.