Atlas FDA

Eversense Continuous Glucose Monitoring System

FDA premarket approval P160048/S010 · decided 2019-07-24

Approval details

PMA number
P160048
Supplement
S010
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Eversense Continuous Glucose Monitoring System
Generic name
Sensor, glucose, implanted, non-adjunctive use
Applicant
Senseonics, Incorporated
Date received
2019-06-24
Decision date
2019-07-24
Days to decision
30 days
Decision code
OK30
Product code
QHJ
Advisory committee
Clinical Chemistry
Expedited review
No
Location
Germantown, MD
Statement
Modification of equipment and processes used to encase the Eversense sensor. The Eversense sensor is a component of the Eversense Continuous Glucose Monitoring system.

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510(k) clearances by this applicant

RecordFirmDate
Eversense 365 Continuous Glucose Monitoring (CGM) System (K241335)Senseonics, Incorporated2024-09-16
Eversense AP CGM System (DEN230052)Senseonics, Incorporated2024-04-29