510(k) K011020

Device
DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBER
Applicant
Denver Biomedicals, Inc.
510(k) number
K011020
Product code
KPM
Decision
Substantially Equivalent (SESE)
Decision date
2001-06-01
Date received
2001-04-04
Regulation
876.5955
Classification name
Shunt, Peritoneal
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
NANCY SAUER
Address
401 Spruce St. Louisville CO US 80027 80027

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code KPM#

510(k), Device, Applicant table
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K012235DENVER PLEURAL EFFUSION SHUNT AND DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBERDenver Biomedical, Inc.2001-10-04
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K973129DENVER ASCITES SHUNTS, DENVER ASCITES SHUNT PERCUTANEOUS ACCESS KITSDenver Biomaterials, Inc.1998-03-17
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K894756DENVER PERITONEO-VENUS SHUNTCodman & Shurtleff, Inc.1989-09-29
K880570DENVER PLEURO-PERITONEAL SHUNTCodman & Shurtleff, Inc.1988-06-20
K880401DENVER PERITONEO-VENOUS SHUNTCodman & Shurtleff, Inc.1988-05-31
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