KTD — Orthosis, Abdominal Class I
FDA Device Classification
Classification Details
- Product Code
- KTD
- Device Class
- Class I
- Regulation Number
- 890.3490
- Submission Type
- Review Panel
- PM
- Medical Specialty
- Physical Medicine
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K823663 | warm and form, orthopedic materials | ABDOMINAL BINDER | December 30, 1982 |
| K823164 | warm and form, orthopedic materials | ABDOMINAL BINDER | November 16, 1982 |
| K780229 | biomet | ABDOMINAL BELT | March 2, 1978 |