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

BlueStar Rx

K Number: K193654 · Decision Apr 7, 2020
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
47
Applicant Total
11
Review Days
99

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Basic Information

Device Name
BlueStar Rx
K Number
K193654
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Welldoc, Inc.
Date Received
December 30, 2019
Decision Date
April 7, 2020
Product Code
MRZ
Advisory Committee
General Hospital
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
MRZ Accessories, Pump, Infusion

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Other Clearances by Welldoc, Inc.

K Number Device Name
K222888 BlueStar CGM insulin dose calculator
K230813 BlueStar and BlueStar Rx
K203434 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
Search all 11 clearances from Welldoc, Inc. →