FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇳 India
Sodium Chloride Inhalation Solution, USP 0.9%, 3% & 7%
K Number: K232523
·
Decision Apr 10, 2024
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
507
Applicant Total
1
Review Days
236
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Basic Information
- Device Name
- Sodium Chloride Inhalation Solution, USP 0.9%, 3% & 7%
- K Number
- K232523
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5630
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Mankind Pharma Limited
- Date Received
- August 18, 2023
- Decision Date
- April 10, 2024
- 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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