McKesson 141-2500-2
by Mckesson Medical-Surgical Inc.
McKesson 141-2500-2 is a diagnostic spirometer (FDA Class II; FDA product code BZG, Spirometer, Diagnostic) made by Mckesson Medical-Surgical Inc., cleared under FDA 510(k) K161536 on 5 Jan 2017 and listed in FDA GUDID since 4 Aug 2017 (UDI-DI 10612479220451), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10612479220451 | Date4 Aug 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK161536 | Date5 Jan 2017 | StatusActive |
Official records
- AccessGUDID record 10612479220451
- FDA 510(k) database K161536
Across registries
- FDA 510(k) K161536 decided 5 Jan 2017 Active
- FDA GUDID UDI-DI 10612479220451 listed 4 Aug 2017 Listed
Timeline
- Cleared FDA 510(k) K161536
- Listed FDA GUDID 10612479220451
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- McKesson
- Generic name
- Diagnostic spirometer, professional
- Model / reference
- 141-2500-2
- Description
- EasyOne Air Spirometry System
- Primary DI / UDI-DI
- 10612479220451
- 510(k) Number
- FDA product code
- BZG
- GMDN term
- Diagnostic spirometer, professional
- Device class
- Class II
- Regulation number
- 868.1840
- GUDID distribution status
- In Commercial Distribution
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