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510(k) K062047

Device
ADAPTABLE MONOPOLAR ADAPTABLE AND/OR RETRACTABLE ELECTRODES
Applicant
PAJUNK GmbH Medizintechnologie
510(k) number
K062047
Product code
GEI
Decision
Substantially Equivalent (SESE)
Decision date
2006-10-05
Date received
2006-07-20
Regulation
878.4400
Classification name
Electrosurgical, Cutting & Coagulation & Accessories
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
CHRISTIAN QUASS
Address
Karl-Hall-Strasse 01 Geisingen DE 78187 78187

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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