FDA.reportPublic FDA data

510(k) K022047

Device
PHLEBOTEST 2000
Applicant
Osborn Medical Corp.
510(k) number
K022047
Product code
JOM
Decision
Substantially Equivalent (SESE)
Decision date
2002-11-04
Date received
2002-06-24
Regulation
870.2780
Classification name
Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
BILL DAVIS
Address
100 W. Main Utica MN US 55979 55979

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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