FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ABLE GENERATION DESK
K Number: K923751
·
Decision Jan 29, 1993
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
34
Applicant Total
4
Review Days
185
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Basic Information
- Device Name
- ABLE GENERATION DESK
- K Number
- K923751
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.3750
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- The Able Generation, Inc.
- Date Received
- July 28, 1992
- Decision Date
- January 29, 1993
- Product Code
- INW
- 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 |
|---|---|---|---|
| INW | Table, Mechanical | FDA class 1 | Physical Medicine |
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