FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
HUNTLEIGH BETA II HM85
K Number: K870681
·
Decision Mar 4, 1987
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
101
Applicant Total
23
Review Days
13
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Basic Information
- Device Name
- HUNTLEIGH BETA II HM85
- K Number
- K870681
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5550
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Huntleigh Technology, Inc.
- Date Received
- February 19, 1987
- Decision Date
- March 4, 1987
- Product Code
- FNM
- 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 |
|---|---|---|---|
| FNM | Mattress, Air Flotation, Alternating Pressure | FDA class 2 | General Hospital |
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