510(k) K951660

DYNAREX GAUZE SPONGE by Dynarex Corp. — Product Code EFQ

K951660 is an FDA 510(k) premarket notification submitted by Dynarex Corp. for the device "DYNAREX GAUZE SPONGE". The FDA issued a decision of Substantially Equivalent on May 9, 1995. 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
May 9, 1995
Date Received
April 10, 1995
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