Medline DYNJ759ELB
Medline DYNJ759ELB is a pulmonary function testing filter/mouthpiece (FDA Class II; FDA product code BZG, Spirometer, Diagnostic) made by Medline Industries, Inc., cleared under FDA 510(k) K042758 on 29 Aug 2005 and listed in FDA GUDID since 14 Jul 2021 (UDI-DI 10888277652439), 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 | Number10888277652439 | Date14 Jul 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK042758 | Date29 Aug 2005 | StatusActive |
Official records
- AccessGUDID record 10888277652439
- FDA 510(k) database K042758
Across registries
- FDA 510(k) K042758 decided 29 Aug 2005 Active
- FDA GUDID UDI-DI 10888277652439 listed 14 Jul 2021 Listed
Timeline
- Cleared FDA 510(k) K042758
- Listed FDA GUDID 10888277652439
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Medline
- Generic name
- Pulmonary function testing filter/mouthpiece
- Model / Ref / Catalog
- DYNJ759ELB
- Primary DI / UDI-DI
- 10888277652439
- 510(k) Number
- FDA product code
- BZG
- GMDN term
- Pulmonary function testing filter/mouthpiece
- Device class
- Class II
- Regulation number
- 868.1840
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Pulmonary function testing filter/mouthpiece.