510(k) K933308

DYNAREX GAUZE SPONGE OR PADS by Dynarex Corp. — Product Code EFQ

K933308 is an FDA 510(k) premarket notification submitted by Dynarex Corp. for the device "DYNAREX GAUZE SPONGE OR PADS". The FDA issued a decision of Substantially Equivalent on December 22, 1993. 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
December 22, 1993
Date Received
July 7, 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