510(k) K833732
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