510(k) K960388

DYNAREX NON-WOVEN SPONGE by Dynarex Corp. — Product Code EFQ

K960388 is an FDA 510(k) premarket notification submitted by Dynarex Corp. for the device "DYNAREX NON-WOVEN SPONGE". The FDA issued a decision of Substantially Equivalent on April 1, 1996. The device falls under product code EFQ (Gauze/Sponge, Internal), a Class U device. Dynarex Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 1, 1996
Date Received
January 26, 1996
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