FDA.reportPublic FDA data

510(k) K781792

Device
Pressurizer, Exeter Cement
Applicant
HOWMEDICA CORP.
510(k) number
K781792
Product code
KIZ
Decision
Substantially Equivalent (SESE)
Decision date
1979-02-08
Date received
1978-10-25
Regulation
864.2240
Classification name
Dish, Tissue Culture
Medical specialty
Hematology
Review panel
Hematology
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code KIZ#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K890542MULTIWELL CULTURE PLATE INSERTSBd Becton Dickinson Vacutainer Systems Preanalytic1989-02-14
K873891TISSUE CULTURE DISHESNunc, Inc.1987-11-25
K871483TISSUE CULTURE/BACTERIOLOGICAL PETRI DISHESIsratech Marketing Corp.1987-04-29
K854724CEKK-ADHESIVE MATRIX-MULTIPLE WELL PLATE CAM-PLATELifetrac, Inc.1985-12-13
K853634CORNING CELL WELLS-MULTIPLE WELL PLATESCorning Medical & Scientific1985-09-16
K821687REMOVAWELL TISSUE CULTURE PLATE W/LIDDynatech Corp.1982-06-24
K790958120 WELL HISTO-PLATEDynatech Laboratories, Inc.1979-06-28