510(k) K881395

GAUZE AND LAP SPONGES -STERILE & NON-STERILE by A Plus International, Inc. — Product Code EFQ

K881395 is an FDA 510(k) premarket notification submitted by A Plus International, Inc. for the device "GAUZE AND LAP SPONGES -STERILE & NON-STERILE". The FDA issued a decision of Substantially Equivalent on April 28, 1988. The device falls under product code EFQ (Gauze/Sponge, Internal), a Class U device. A Plus International, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 28, 1988
Date Received
April 4, 1988
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