510(k) K903358

ADVANCE LAPAROTOMY SPONGE, LAP SPONGE by Advance Medical Designs, Inc. — Product Code GDY

K903358 is an FDA 510(k) premarket notification submitted by Advance Medical Designs, Inc. for the device "ADVANCE LAPAROTOMY SPONGE, LAP SPONGE". The FDA issued a decision of Substantially Equivalent on November 29, 1990. The device falls under product code GDY (Gauze/Sponge, Internal, X-Ray Detectable), a Class I device regulated under 21 CFR 878.4450. Advance Medical Designs, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 29, 1990
Date Received
July 26, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Gauze/Sponge, Internal, X-Ray Detectable
Device Class
Class I
Regulation Number
878.4450
Review Panel
SU
Submission Type