510(k) K830202

COTTON BALLS, X-RAY OPAQUED STRUNG & NON by American Medical Disposable, Inc. — Product Code GDY

K830202 is an FDA 510(k) premarket notification submitted by American Medical Disposable, Inc. for the device "COTTON BALLS, X-RAY OPAQUED STRUNG & NON". The FDA issued a decision of Substantially Equivalent on February 23, 1983. The device falls under product code GDY (Gauze/Sponge, Internal, X-Ray Detectable), a Class I device regulated under 21 CFR 878.4450. American Medical Disposable, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 23, 1983
Date Received
January 20, 1983
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