FDA 510(k)
FDA class 1
Substantially Equivalent
🇨🇦 Canada
MEDI-PLINTH
K Number: K924905
·
Decision Feb 16, 1993
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
101
Applicant Total
4
Review Days
140
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Basic Information
- Device Name
- MEDI-PLINTH
- K Number
- K924905
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.3760
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Medi-Man Rehabilitation Products, Inc.
- Date Received
- September 29, 1992
- Decision Date
- February 16, 1993
- Product Code
- INQ
- 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 |
|---|---|---|---|
| INQ | Table, Powered | FDA class 1 | Physical Medicine |
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