Identity
- Trade Name
- Sodium Chloride Inhalation Solution, USP 3% FDA UDI
- Generic Name
- Inhalation therapy saline solution, hypertonic FDA UDI
- Model / Reference
- 900330 FDA UDI
Identifiers
- Catalog Number
- 0487-9003-30 FDA UDI
- Primary DI / UDI-DI
- 00304879003309 FDA UDI
- 510(k) Number
- K120051 FDA UDI
- FDA Product Code
- CAF FDA UDI
- GMDN Term
- Inhalation therapy saline solution, hypertonic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5630 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Inhalation therapy saline solution, hypertonic
Sodium Chloride Inhalation Solution, USP 3% by Nephron Pharmaceuticals Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Inhalation therapy saline solution, hypertonic.
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- Sodium Chloride Inhalation Solution, USP, 3.5% 4mL UDV — RITEDOSE PHARMACEUTICALS, LLC · Class II
Cleared under the same submission
K120051 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Nephron Pharmaceuticals Corp.
Sources (1)
- FDA UDI 298a32cd-d47e-4372-8e73-e60a2e02c53a 35 fields · synced May 30, 2026