510(k) K052416

Device
PERIPRO PATCH
Applicant
Hancock/Jaffe Laboratories
510(k) number
K052416
Product code
DXZ
Decision
Substantially Equivalent (SESE)
Decision date
2005-10-25
Date received
2005-09-02
Regulation
870.3470
Classification name
Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
N

Applicant Contact#

Contact
SUE MONTOYA
Address
2807 Mcgaw Ave. Irvine CA US 92614 92614

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code DXZ#

510(k), Device, Applicant table
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