FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
THE MURRAY MOBILIFT(TM)
K Number: K895677
·
Decision Oct 26, 1990
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
20
Applicant Total
4
Review Days
401
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Basic Information
- Device Name
- THE MURRAY MOBILIFT(TM)
- K Number
- K895677
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5500
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Medical/Surgical Specialties, Ltd.
- Date Received
- September 20, 1989
- Decision Date
- October 26, 1990
- Product Code
- FNG
- 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 |
|---|---|---|---|
| FNG | Lift, Patient, Ac-Powered | FDA class 2 | General Hospital |
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