FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
WHEELED STRETCHER
K Number: K900872
·
Decision May 18, 1990
Classifications
1
FEI Numbers
112
Registration Numbers
112
Same Product Code
49
Applicant Total
2
Review Days
81
Basic Information
- Device Name
- WHEELED STRETCHER
- K Number
- K900872
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.6910
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- HOSPITAL SUPPLY CO., INC.
- Date Received
- February 26, 1990
- Decision Date
- May 18, 1990
- 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 HOSPITAL SUPPLY CO., INC.
| K Number | Device Name | ||
|---|---|---|---|
| K900873 | PEDIATRIC HOSPITAL BED | May 18, 1990 | Substantially Equivalent |