FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ROMFLEX REHABILITATION EQUIPMENT
K Number: K905299
·
Decision Dec 31, 1990
Classifications
1
FEI Numbers
113
Registration Numbers
113
Same Product Code
159
Applicant Total
4
Review Days
33
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Basic Information
- Device Name
- ROMFLEX REHABILITATION EQUIPMENT
- K Number
- K905299
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.5380
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Applicant
- Dyna Flex, Intl.
- Date Received
- November 28, 1990
- Decision Date
- December 31, 1990
- Product Code
- BXB
- Advisory Committee
- Physical Medicine
- Review Advisory Committee
- PM
- 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 |
|---|---|---|---|
| BXB | Exerciser, Powered | FDA class 1 | Physical Medicine |
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