FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ICEL ULTRASONIC NEBULIZER MODELS PU 12000 AND PU 12300
K Number: K951259
·
Decision Jun 20, 1995
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
507
Applicant Total
1
Review Days
91
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Basic Information
- Device Name
- ICEL ULTRASONIC NEBULIZER MODELS PU 12000 AND PU 12300
- K Number
- K951259
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5630
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Impulso Trading Co.
- Date Received
- March 21, 1995
- Decision Date
- June 20, 1995
- 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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