510(k) K833732

NON WETTING UNDERCAST PADDING by American Medical Disposable, Inc. — Product Code ITG

K833732 is an FDA 510(k) premarket notification submitted by American Medical Disposable, Inc. for the device "NON WETTING UNDERCAST PADDING". The FDA issued a decision of Substantially Equivalent on December 12, 1983. The device falls under product code ITG (Bandage, Cast), a Class I device regulated under 21 CFR 890.3025. American Medical Disposable, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 12, 1983
Date Received
October 25, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bandage, Cast
Device Class
Class I
Regulation Number
890.3025
Review Panel
PM
Submission Type