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

WELLDOC DIABETES MANAGER SYSTEM AND DIABETES MANAGER RX SYSTEM

K Number: K112370 · Decision Oct 14, 2011
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
47
Applicant Total
11
Review Days
58

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
WELLDOC DIABETES MANAGER SYSTEM AND DIABETES MANAGER RX SYSTEM
K Number
K112370
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Welldoc, Inc.
Date Received
August 17, 2011
Decision Date
October 14, 2011
Product Code
MRZ
Advisory Committee
General Hospital
Review Advisory Committee
HO
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MRZ), ordered by most recent decision date.

View all

Other Clearances by Welldoc, Inc.

K Number Device Name
K222888 BlueStar CGM insulin dose calculator
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
K100066 DIABETESMANAGER SYSTEM, DIABETESMANAGER-RX SYSTEM MODEL VERSION 1.1
Search all 11 clearances from Welldoc, Inc. →