FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ALLEN UNIVERSAL STIRRUP
K Number: K860177
·
Decision Feb 11, 1986
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
19
Applicant Total
3
Review Days
25
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Basic Information
- Device Name
- ALLEN UNIVERSAL STIRRUP
- K Number
- K860177
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4950
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Edgewater Medical Equipment Systems
- Date Received
- January 17, 1986
- Decision Date
- February 11, 1986
- Product Code
- BWN
- 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 |
|---|---|---|---|
| BWN | Table And Attachments, Operating-Room | FDA class 1 | General, Plastic Surgery |
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