510(k) K034015

Device
EARLOOP PROCEDURE MASK
Applicant
Medipack Medical Packaging Mfg. Co.
510(k) number
K034015
Product code
FXX
Decision
Substantially Equivalent (SESE)
Decision date
2004-02-20
Date received
2003-12-24
Regulation
878.4040
Classification name
Mask, Surgical
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
N

Related Records

Applicant Contact

Contact
ANTONIO L GIACCIO
Address
1202 S. Rte. 31 Mc Henry IL US 60050 60050

FDA Registration Numbers

Source Documents

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code FXX

510(k)DeviceApplicantDecision date
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