510(k) K802384

CENTRAL VENOUS CATHETER DRESSING TRAY by American Medical Disposable, Inc. — Product Code FPX

K802384 is an FDA 510(k) premarket notification submitted by American Medical Disposable, Inc. for the device "CENTRAL VENOUS CATHETER DRESSING TRAY". The FDA issued a decision of Substantially Equivalent on November 12, 1980. The device falls under product code FPX (Strip, Adhesive, Closure, Skin), a Class I device regulated under 21 CFR 880.5240. American Medical Disposable, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 12, 1980
Date Received
October 2, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Strip, Adhesive, Closure, Skin
Device Class
Class I
Regulation Number
880.5240
Review Panel
SU
Submission Type