FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
AQUA-BLANKET HYPER/HYPOHERMIA BLANKET
K Number: K890852
·
Decision Apr 14, 1989
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
92
Applicant Total
3
Review Days
52
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Basic Information
- Device Name
- AQUA-BLANKET HYPER/HYPOHERMIA BLANKET
- K Number
- K890852
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 890.5720
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Applicant
- Ati
- Date Received
- February 21, 1989
- Decision Date
- April 14, 1989
- Product Code
- ILO
- 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 |
|---|---|---|---|
| ILO | Pack, Hot Or Cold, Water Circulating | FDA class 2 | Physical Medicine |
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