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510(k) K822254

Device
ELECTRIC CORD FOR ENDOSCOPE
Applicant
KELLEHER CORP.
510(k) number
K822254
Product code
FFZ  
Decision
Substantially Equivalent (SESE)
Decision date
1982-08-20
Date received
1982-07-29
Regulation
876.1500
Classification name
Cord, Electric, For Endoscope
Medical specialty
Gastroenterology/Urology
Review panel
Gastroenterology/Urology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

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

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code FFZ  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K111013ACEMSandhill Scientific, Inc.2011-12-19
K782046C-CORDConcept, Inc.1979-01-10

Legacy Summary#

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FDA Review#

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