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510(k) K780181

Device
GLOVES, FLOOR
Applicant
TILLOTSON RUBBER CO., INC.
510(k) number
K780181
Product code
FML  
Decision
Substantially Equivalent (SESE)
Decision date
1978-02-21
Date received
1978-02-03
Regulation
880.6140
Classification name
Chair, Blood Donor
Medical specialty
General Hospital
Review panel
General Hospital
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 FML  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K842517UNILET LANCETUlster Scientific, Inc.1984-09-20

Legacy Summary#

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FDA Review#

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