510(k) K884967

Device
BACTIGEN(R) H. INFLUENZAE TYPE B
Applicant
ARMKEL, LLC.
510(k) number
K884967
Product code
GRP  
Decision
Substantially Equivalent (SESE)
Decision date
1989-02-07
Date received
1988-11-30
Regulation
866.3300
Classification name
Antisera, All Types, H. Influenza
Medical specialty
Microbiology
Review panel
Microbiology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
ANN MACLEARIE
Address
Half Acre Rd. P.O. Box 1001 Cranbury NJ US 08512 08512

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code GRP  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K854490IMMUNOSCAN DIRECT HEMOPHILUS INFLUENZAE TYPE B TESAmerican Micro Scan1985-12-27
K831525H-FLU B ELISA TESTSeragen Diagnostics, Inc.1983-09-29
K823348H. INFLUENZA B ANTISERA FOR CIEDiagnostica, Inc.1982-12-28
K821266BBL DIRECTIGEN MENINGITIS TEST KITBd Becton Dickinson Vacutainer Systems Preanalytic1982-06-01
K820192HAEMOPHILUS INFLUENZAE TYPE B ANTISERUMHyland Therapeutic Div., Travenol Laboratories1982-03-11

Legacy Summary#

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FDA Review#

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