510(k) K946326

DUTEX GAUZE BANDAGE by Dumex Medical Surgical Products, Ltd. — Product Code EFQ

K946326 is an FDA 510(k) premarket notification submitted by Dumex Medical Surgical Products, Ltd. for the device "DUTEX GAUZE BANDAGE". The FDA issued a decision of Substantially Equivalent on January 24, 1995. The device falls under product code EFQ (Gauze/Sponge, Internal), a Class U device. Dumex Medical Surgical Products, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 24, 1995
Date Received
December 22, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Gauze/Sponge, Internal
Device Class
Class U
Regulation Number
Review Panel
SU
Submission Type