Atlas FDA

BACT/ALERT CSR

FDA 510(k) clearance K003104 · decided 2000-10-20

Clearance details

K-number
K003104
Device name
BACT/ALERT CSR
Applicant
Organon Teknika Corp.
Decision
Substantially Equivalent
Date received
2000-08-29
Decision date
2000-10-20
Days to decision
52 days
Clearance type
Traditional
Product code
LJF
Device class
1
Regulation number
866.2560
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Durham, NC, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
ARTIMICROBIAL REMOVAL DEVICE (K830372)Marion Laboratories, Inc.1983-04-08
BACTEC 170 TRYPTIC SOY BROTH W/RESINS (K830363)Bd Becton Dickinson Vacutainer Systems Preanalytic1983-03-24
ANTIMICROBIAL REMOVAL DEVICE (ARD) (K822344)Marion Laboratories, Inc.1982-08-25

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
HEPANOSTIKA(TM) ANTI-HAV MIDROELISA SYSTEM (P830018/S001)Organon Teknika Corp.1990-03-21
HEPANOSTIKA(TM) HBEAG/ANTI HBE MICROELISA(TM) SYST (P840070/S001)Organon Teknika Corp.1990-03-21
9EPANOSTIKA(TM) ANTI-HAV IGM (P830017/S001)Organon Teknika Corp.1990-03-21
AUTOBAC MIC TEST SYSTEM (N50524/S033)Organon Teknika Corp.1990-01-22
AUTOBAC MIC TEST SYSTEM (N50524/S035)Organon Teknika Corp.1989-12-07
AUTOBAC MIC TEST SYSTEM (N50524/S032)Organon Teknika Corp.1989-06-13
HEPANOSTIKA(TM) ANTI-HAV MIDROELISA SYSTEM (P830018)Organon Teknika Corp.1989-02-06
AUTOBAC MIC TEST SYSTEM (N50524/S031)Organon Teknika Corp.1988-12-28