FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
RITTERMODEL 75 EVOLUTION UNIV POW EXAM TABLE/ACCES
K Number: K926463
·
Decision Oct 21, 1994
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
34
Applicant Total
31
Review Days
666
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Basic Information
- Device Name
- RITTERMODEL 75 EVOLUTION UNIV POW EXAM TABLE/ACCES
- K Number
- K926463
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4960
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Midmark Corp.
- Date Received
- December 24, 1992
- Decision Date
- October 21, 1994
- Product Code
- FQO
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| FQO | Table, Operating-Room, Ac-Powered | FDA class 1 | General, Plastic Surgery |
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