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510(k) K760389

Device
CANNULA, IV
Applicant
B. BRAUN INSTRUMENTS
510(k) number
K760389
Product code
FGY  
Decision
Substantially Equivalent (SESE)
Decision date
1976-11-02
Date received
1976-08-05
Regulation
878.4200
Classification name
Cannula, Injection
Medical specialty
General & Plastic Surgery
Review panel
General & Plastic Surgery
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 FGY  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K822201EAR CANNULASKelleher Corp.1982-10-06

Legacy Summary#

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FDA Review#

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