FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
MEDPRO FLOTATION SYSTEM
K Number: K771824
·
Decision Oct 19, 1977
Classifications
1
FEI Numbers
154
Registration Numbers
154
Same Product Code
7
Applicant Total
4
Review Days
22
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Basic Information
- Device Name
- MEDPRO FLOTATION SYSTEM
- K Number
- K771824
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.5150
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Medpro, Inc.
- Date Received
- September 27, 1977
- Decision Date
- October 19, 1977
- Product Code
- IKY
- 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 |
|---|---|---|---|
| IKY | Mattress, Flotation Therapy, Non-Powered | FDA class 1 | General Hospital |
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