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510(k) K912693

Device
POST OPERATIVE SPONGE
Applicant
ULTI-MED INTL., INC.
510(k) number
K912693
Product code
GER  
Decision
Substantially Equivalent (SESE)
Decision date
1991-10-04
Date received
1991-06-18
Regulation
510(k) Premarket Notification
Classification name
Gauze, External (with Drug/biologic/animal Source Material)
Medical specialty
510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration   Follow FDA En Español Search FDA   Home Food Drugs Medical Devices
Review panel
General & Plastic Surgery
Device class
1
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
DAVID INSCO
Address
1688 Glen Ellyn Rd. Glendale Hts. IL US 60139 60139

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Legacy Summary#

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FDA Review#

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