Ez Flo NEZ22200
by Air-Tite Products Company, Inc.
Ez Flo NEZ22200 is a Class II device made by Air-Tite Products Company, Inc., cleared under FDA 510(k) K112057 on 14 Dec 2011 and listed in FDA GUDID since 15 Apr 2020 (UDI-DI 10850017403168), 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 | Number10850017403168 | Date15 Apr 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK112057 | Date14 Dec 2011 | StatusActive |
Official records
- AccessGUDID record 10850017403168
- FDA 510(k) database K112057
Across registries
- FDA 510(k) K112057 decided 14 Dec 2011 Active
- FDA GUDID UDI-DI 10850017403168 listed 15 Apr 2020 Listed
Timeline
- Cleared FDA 510(k) K112057
- Listed FDA GUDID 10850017403168
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Ez Flo
- Generic name
- Hypodermic needle, single-use
- Model / Ref / Catalog
- NEZ22200
- Primary DI / UDI-DI
- 10850017403168
- 510(k) Number
- FDA product code
- FMI
- GMDN term
- Hypodermic needle, single-use
- Device class
- Class II
- Regulation number
- 880.5570
- GUDID distribution status
- In Commercial Distribution
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