510(k) K872809

GAUZE CHERRY SPONGE by American Silk Sutures, Inc. — Product Code GDY

K872809 is an FDA 510(k) premarket notification submitted by American Silk Sutures, Inc. for the device "GAUZE CHERRY SPONGE". The FDA issued a decision of Substantially Equivalent on August 4, 1987. The device falls under product code GDY (Gauze/Sponge, Internal, X-Ray Detectable), a Class I device regulated under 21 CFR 878.4450. American Silk Sutures, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 4, 1987
Date Received
July 14, 1987
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