510(k) K945021

FLUFF GAUZE SPONGE by Clinical Resources, Inc. — Product Code EFQ

K945021 is an FDA 510(k) premarket notification submitted by Clinical Resources, Inc. for the device "FLUFF GAUZE SPONGE". The FDA issued a decision of Substantially Equivalent on December 23, 1994. The device falls under product code EFQ (Gauze/Sponge, Internal), a Class U device. Clinical Resources, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 23, 1994
Date Received
October 12, 1994
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