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

BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM-PIPERCILLIN (GN) 0.5-128 UG/ML

K Number: K041572 · Decision Aug 12, 2004
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
288
Applicant Total
6
Review Days
59

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 PHOENIX AUTOMATED MICROBIOLOGY SYSTEM-PIPERCILLIN (GN) 0.5-128 UG/ML
K Number
K041572
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.1645
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Becton, Dickinson and Co.
Date Received
June 14, 2004
Decision Date
August 12, 2004
Product Code
LON
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
LON System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

Similar 510(k) Clearances

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

View all

Other Clearances by Becton, Dickinson and Co.

K Number Device Name
K152874 BD Veritor System for the Rapid Detection of Flu A + B Laboratory kit
K152870 BD Veritor System for the Rapid Detection of Flu A + B CLIA waived kit
K100005 BD PEN NEEDLE
K010890 BD ULTRA-FINE II INSULIN SYRINGE-MINI NEEDLE, MODEL 30G * 3/16 (5MM)
K010572 BD VISIDRAPE OPHTHALMIC DRAPES; BD VISIFLEX INCISE DRAPE