FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
SANITAS PATIENT LIFT
K Number: K930625
·
Decision Sep 13, 1993
Classifications
1
FEI Numbers
206
Registration Numbers
207
Same Product Code
12
Applicant Total
3
Review Days
217
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Basic Information
- Device Name
- SANITAS PATIENT LIFT
- K Number
- K930625
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.5510
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Dutton-Lainson Co.
- Date Received
- February 8, 1993
- Decision Date
- September 13, 1993
- Product Code
- FSA
- 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 |
|---|---|---|---|
| FSA | Lift, Patient, Non-Ac-Powered | FDA class 1 | General Hospital |
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