FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
STRETCHER, WHEELED, MECHANICAL
K Number: K873181
·
Decision Oct 9, 1987
Classifications
1
FEI Numbers
105
Registration Numbers
105
Same Product Code
49
Applicant Total
2
Review Days
58
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Basic Information
- Device Name
- STRETCHER, WHEELED, MECHANICAL
- K Number
- K873181
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.6910
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Cambridge Technologies, Inc.
- Date Received
- August 12, 1987
- Decision Date
- October 9, 1987
- Product Code
- FPO
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| FPO | Stretcher, Wheeled | FDA class 2 | General Hospital |
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Other Clearances by Cambridge Technologies, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K882493 | ROD, IRRIGATOR SUPPORTING, TELESCOPING TYPE | Jul 19, 1988 | Substantially Equivalent |