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510(k) K770158

Device
HEMOSTAT
Applicant
DERINGER-NEY INC.
510(k) number
K770158
Product code
EMD  
Decision
Substantially Equivalent (SESE)
Decision date
1977-01-31
Date received
1977-01-24
Regulation
872.4565
Classification name
Hemostat, Surgical
Medical specialty
Dental
Review panel
Dental
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 EMD  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K920883HEMOSTAT, SURGICAL (VARIOUS TYPES)S.T.S Instruments1992-03-13

Legacy Summary#

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FDA Review#

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