510(k) K936095

GAUZE SPONGE by Dukal Corp. — Product Code EFQ

K936095 is an FDA 510(k) premarket notification submitted by Dukal Corp. for the device "GAUZE SPONGE". The FDA issued a decision of Substantially Equivalent on February 2, 1994. The device falls under product code EFQ (Gauze/Sponge, Internal), a Class U device. Dukal Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 2, 1994
Date Received
December 22, 1993
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