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

IGLUCOSE SYSTEM

K Number: K111932 · Decision Nov 10, 2011
Classifications
1
FEI Numbers
168
Registration Numbers
169
Same Product Code
507
Applicant Total
1
Review Days
125

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
IGLUCOSE SYSTEM
K Number
K111932
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1345
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Positiveid Corporation
Date Received
July 8, 2011
Decision Date
November 10, 2011
Product Code
NBW
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
NBW System, Test, Blood Glucose, Over The Counter

Similar 510(k) Clearances

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

View all