FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
NEBULIZER, MOLEL 503, PART #17068
K Number: K771105
·
Decision Jul 5, 1977
Classifications
1
FEI Numbers
187
Registration Numbers
188
Same Product Code
503
Applicant Total
55
Review Days
15
Basic Information
- Device Name
- NEBULIZER, MOLEL 503, PART #17068
- K Number
- K771105
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5630
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- HOSPAL MEDICAL CORP.
- Date Received
- June 20, 1977
- Decision Date
- July 5, 1977
- 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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