510(k) K083730

Device
ISOLAZ
Applicant
AESTHERA CORPORATION
510(k) number
K083730
Product code
GEX  
Decision
Substantially Equivalent (SESE)
Decision date
2009-01-09
Date received
2008-12-16
Regulation
878.4810
Classification name
Powered Laser Surgical Instrument
Medical specialty
General & Plastic Surgery
Review panel
General & Plastic Surgery
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
PAMELA M BUCKMAN
Address
1070 Concord Ave. Suite 230 Concord CA US 94520 94520

FDA Registration Numbers

Source Documents

510(k) summary PDF

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Legacy Summary

summary

FDA Review

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