510(k) K803116

HEAVY DRAINAGE PACK by American Medical Disposable, Inc. — Product Code GEC

K803116 is an FDA 510(k) premarket notification submitted by American Medical Disposable, Inc. for the device "HEAVY DRAINAGE PACK". The FDA issued a decision of Substantially Equivalent on January 28, 1981. The device falls under product code GEC (Brush, Scrub, Operating-Room), 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
January 28, 1981
Date Received
December 10, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Brush, Scrub, Operating-Room
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type