FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
FT MODEL TABLE W/ELECTRIC HI LO OPTION E
K Number: K925563
·
Decision May 26, 1993
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
101
Applicant Total
1
Review Days
204
Basic Information
- Device Name
- FT MODEL TABLE W/ELECTRIC HI LO OPTION E
- K Number
- K925563
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.3760
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- PRO MED MFG., INC.
- Date Received
- November 3, 1992
- Decision Date
- May 26, 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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