510(k) K012419

Device
CONFORM SHEETING, MODEL IGEL
Applicant
Implantech Associates, Inc.
510(k) number
K012419
Product code
MDA
Decision
Substantially Equivalent (SESE)
Decision date
2001-10-24
Date received
2001-07-30
Regulation
878.4025
Classification name
Elastomer, Silicone, For Scar Management
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
1
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
N

Related Records

Applicant Contact

Contact
STEPHEN MEADE
Address
2064 Eastman Ave., Unit 101 Ventura CA US 93003 93003

FDA Registration Numbers

Source Documents

510(k) summary PDF not indicated by FDA

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