FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

BACT/ALERT FAN CULTURE BOTTLE

K Number: K944594 · Decision Feb 17, 1995
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
66
Applicant Total
130
Review Days
151

Basic Information

Device Name
BACT/ALERT FAN CULTURE BOTTLE
K Number
K944594
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2560
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ORGANON TEKNIKA CORP.
Date Received
September 19, 1994
Decision Date
February 17, 1995
Product Code
MDB
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
MDB System, Blood Culturing

Similar 510(k) Clearances

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

View all

Other Clearances by ORGANON TEKNIKA CORP.

K Number Device Name
K003104 BACT/ALERT CSR
K000492 MDA D-DIMER
K000378 BACT/ALERT MB CULTURE BOTTLE
K994343 BACT/ALERT SV
K993423 BACT/ALERT SA
K993421 BACT/ALERT SN
K993576 BACT/ALERT MP PROCESS BOTTLE
K992432 BACT/ALERT FN
K983762 NUCLISENS CMV PP67
K992401 BACT/ALERT PF
Search all 130 clearances from ORGANON TEKNIKA CORP. →