FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇦 Canada
MC ACCLAIM Q6000 BED
K Number: K951161
·
Decision May 9, 1995
Classifications
1
FEI Numbers
228
Registration Numbers
228
Same Product Code
69
Applicant Total
3
Review Days
56
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Basic Information
- Device Name
- MC ACCLAIM Q6000 BED
- K Number
- K951161
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5100
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Janco Consulting Services
- Date Received
- March 14, 1995
- Decision Date
- May 9, 1995
- Product Code
- FNL
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| FNL | Bed, Ac-Powered Adjustable Hospital | FDA class 2 | General Hospital |
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