FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
UNIPOWER RECHARGEABLE BATTERY PACK
K Number: K936141
·
Decision Mar 31, 1994
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
6
Applicant Total
3
Review Days
94
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Basic Information
- Device Name
- UNIPOWER RECHARGEABLE BATTERY PACK
- K Number
- K936141
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.2885
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Unipower Corp.
- Date Received
- December 27, 1993
- Decision Date
- March 31, 1994
- Product Code
- BXP
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- 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 |
|---|---|---|---|
| BXP | Transducer, Gas Flow | FDA class 1 | Anesthesiology |
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