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

BD LOGIC BLOOD GLUCOSE MONITOR AND PARADIGM LINK BLOOD GLUCOSE MONITOR

K Number: K041478 · Decision Oct 28, 2004
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
400
Applicant Total
6
Review Days
147

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
BD LOGIC BLOOD GLUCOSE MONITOR AND PARADIGM LINK BLOOD GLUCOSE MONITOR
K Number
K041478
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1345
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Becton Dickinson
Date Received
June 3, 2004
Decision Date
October 28, 2004
Product Code
CGA
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
CGA Glucose Oxidase, Glucose

Similar 510(k) Clearances

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

View all

Other Clearances by Becton Dickinson

K Number Device Name
K243062 BD Intelliport System; BD Intelliport Reader (516230); BD Intelliport Sensor (516229); BD Intelliport Gateway (516232); BD Intelliport Mount (516233); BD Intelliport Charger (516231)
K161810 BD BACTEC Standard/10 Aerobic/F Culture Vials Soybean-Casein Digest Broth in a Plastic Vial
K161306 BD BACTEC Standard Anaerobic/F Culture Vials Soybean-Casein Digest Broth in a Plastic Vial
K113241 BD EMERALD SINGLE USE, HYPODERMIC SYRINGE
K042061 0.9% SODIUM CHLORIDE INJECTION, USP BD POSTFLUSH SF FLUSH SYRINGE