510(k) K970457

DUKAL ABD COMBINE PAD by Dukal Corp. — Product Code EFQ

K970457 is an FDA 510(k) premarket notification submitted by Dukal Corp. for the device "DUKAL ABD COMBINE PAD". The FDA issued a decision of Substantially Equivalent on May 8, 1997. 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
May 8, 1997
Date Received
February 6, 1997
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