McKesson 16-20069
by Mckesson Medical-Surgical Inc.
McKesson 16-20069 is a Class II device made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 18 Jun 2020 (UDI-DI 20612479257805), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number20612479257805 | Date18 Jun 2020 | StatusListed |
Official records
- AccessGUDID record 20612479257805
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- McKesson
- Generic name
- Inhalation therapy saline solution, hypertonic
- Model / reference
- 16-20069
- Primary DI / UDI-DI
- 20612479257805
- FDA product code
- CAF
- GMDN term
- Inhalation therapy saline solution, hypertonic
- Device class
- Class II
- Regulation number
- 868.5630
- GUDID distribution status
- In Commercial Distribution
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