FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CHILLBUSTER PORTABLE ELECTRIC BLANKET SYSTEM, MODEL 8001
K Number: K991684
·
Decision Mar 1, 2000
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
157
Applicant Total
3
Review Days
289
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Basic Information
- Device Name
- CHILLBUSTER PORTABLE ELECTRIC BLANKET SYSTEM, MODEL 8001
- K Number
- K991684
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.5900
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Thermogear, Inc.
- Date Received
- May 17, 1999
- Decision Date
- March 1, 2000
- Product Code
- DWJ
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- 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 |
|---|---|---|---|
| DWJ | System, Thermal Regulating | FDA class 2 | Cardiovascular |
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