510(k) K803119

LARGE WOUND DRESSING KIT by American Medical Disposable, Inc. — Product Code KDD

K803119 is an FDA 510(k) premarket notification submitted by American Medical Disposable, Inc. for the device "LARGE WOUND DRESSING KIT". The FDA issued a decision of Substantially Equivalent on December 30, 1980. The device falls under product code KDD (Kit, Surgical Instrument, Disposable), a Class I device regulated under 21 CFR 878.4800. American Medical Disposable, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 30, 1980
Date Received
December 10, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Kit, Surgical Instrument, Disposable
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type