510(k) K862126

STERILE LAPAROTOMY GAUZE SPONGE by Anago, Inc. — Product Code EFQ

K862126 is an FDA 510(k) premarket notification submitted by Anago, Inc. for the device "STERILE LAPAROTOMY GAUZE SPONGE". The FDA issued a decision of Substantially Equivalent on June 19, 1986. The device falls under product code EFQ (Gauze/Sponge, Internal), a Class U device. Anago, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 19, 1986
Date Received
June 4, 1986
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