FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
WILLIAMS BELT & BOOT
K Number: K891387
·
Decision May 23, 1989
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
12
Applicant Total
4
Review Days
70
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Basic Information
- Device Name
- WILLIAMS BELT & BOOT
- K Number
- K891387
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4950
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Arthro-Medic, Inc.
- Date Received
- March 14, 1989
- Decision Date
- May 23, 1989
- Product Code
- JEB
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| JEB | Table, Surgical With Orthopedic Accessories, Manual | FDA class 1 | General, Plastic Surgery |
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