FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MANGAR BOOSTER
K Number: K905414
·
Decision Mar 5, 1991
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
20
Applicant Total
1
Review Days
92
Basic Information
- Device Name
- MANGAR BOOSTER
- K Number
- K905414
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5500
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- NORTHFLEET MANAGEMENT GROUP, INC.
- Date Received
- December 3, 1990
- Decision Date
- March 5, 1991
- 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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