FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BlueStar CGM insulin dose calculator

K Number: K222888 · Decision Aug 11, 2023
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
4
Applicant Total
11
Review Days
322

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Basic Information

Device Name
BlueStar CGM insulin dose calculator
K Number
K222888
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1358
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Welldoc, Inc.
Date Received
September 23, 2022
Decision Date
August 11, 2023
Product Code
QRX
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
QRX Continuous Glucose Monitor Informed Insulin Dose Calculator

Similar 510(k) Clearances

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Other Clearances by Welldoc, Inc.

K Number Device Name
K230813 BlueStar and BlueStar Rx
K203434 BlueStar Rx
K193654 BlueStar Rx
K190013 WellDoc BlueStar
K162532 WellDoc BlueStar, WellDoc BlueStar Rx
K162225 WellDoc BlueStar (WellDoc DiabetesManager System and DiabetesManager-Rx System
K141273 WELLDOC DIABETESMANAGER SYSTEM AND DIABETESMANAGER- RX SYSTE
K120314 WELLDOC DIABETES MANAGER SYSTEM AND DIABETES MANAGER RX SYSTEM
K112370 WELLDOC DIABETES MANAGER SYSTEM AND DIABETES MANAGER RX SYSTEM
K100066 DIABETESMANAGER SYSTEM, DIABETESMANAGER-RX SYSTEM MODEL VERSION 1.1
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