FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
COMPRESSOR NEBULIZER, MODEL EMG NBA02-XXX SERIES
K Number: K043238
·
Decision Jul 6, 2005
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
507
Applicant Total
11
Review Days
226
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Basic Information
- Device Name
- COMPRESSOR NEBULIZER, MODEL EMG NBA02-XXX SERIES
- K Number
- K043238
- Device Class
- FDA class 2
- Clearance Type
- Abbreviated
- Regulation Number
- 868.5630
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Emg Technology Co., Ltd.
- Date Received
- November 22, 2004
- Decision Date
- July 6, 2005
- Product Code
- CAF
- 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 |
|---|---|---|---|
| CAF | Nebulizer (Direct Patient Interface) | FDA class 2 | Anesthesiology |
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