FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
EVT-5000BX
K Number: K952600
·
Decision Jun 22, 1995
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
101
Applicant Total
5
Review Days
16
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Basic Information
- Device Name
- EVT-5000BX
- K Number
- K952600
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.3760
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- U.S. Table, Inc.
- Date Received
- June 6, 1995
- Decision Date
- June 22, 1995
- 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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