Securegard 1.0
by SafeGard Medical /Hungary/ Gyogyaszati Eszkozgyarto es Forgalmazo Korlatolt Felelossegu Tarsasag 22 variants
Securegard 1.0 (5158P) is a Class II device made by SafeGard Medical /Hungary/ Gyogyaszati Eszkozgyarto es Forgalmazo Korlatolt Felelossegu Tarsasag, cleared under FDA 510(k) K993609 on 17 Mar 2000 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 05999039512453), active as of 22 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 | Number05999039512453 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK993609 | Date17 Mar 2000 | StatusActive |
Official records
- AccessGUDID record 05999039512453
- FDA 510(k) database K993609
Across registries
- FDA 510(k) K993609 decided 17 Mar 2000 Active
- FDA GUDID UDI-DI 05999039512453 listed 24 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K993609
- Listed FDA GUDID 05999039512453
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Securegard
- Generic name
- Metered-delivery hypodermic syringe/needle
- Model / Ref / Catalog
- 1.0, 5158P
- Primary DI / UDI-DI
- 05999039512453
- 510(k) Number
- FDA product code
- MEG
- GMDN term
- Metered-delivery hypodermic syringe/needle
- Device class
- Class II
- Regulation number
- 880.5860
- GUDID distribution status
- In Commercial Distribution