FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
BANDAGE, TRIANGULAR NO. 8068
K Number: K760250
·
Decision Jul 26, 1976
Classifications
1
FEI Numbers
326
Registration Numbers
326
Same Product Code
20
Applicant Total
206
Review Days
7
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Basic Information
- Device Name
- BANDAGE, TRIANGULAR NO. 8068
- K Number
- K760250
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.3640
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Applicant
- Johnson & Johnson Professionals, Inc.
- Date Received
- July 19, 1976
- Decision Date
- July 26, 1976
- Product Code
- ILI
- Advisory Committee
- Physical Medicine
- 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 |
|---|---|---|---|
| ILI | Sling, Arm | FDA class 1 | Physical Medicine |
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