Patient Safe Luer Cap
FDA 510(k) K101708 · Retractable Technologies, Inc.
510(k) numberK101708
Submission
- Device name
- Patient Safe Luer Cap
- Applicant
- Retractable Technologies, Inc.
Little Elm, TX, US - Received
- June 17, 2010
- Decision date
- February 24, 2011
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- FMF – Syringe, Piston
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.5860
- Specialty
- General Hospital
Other 510(k)s with product code FMF
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| K262581 | GraftGun Universal Graft Delivery System (GDS®)FMF · Special | SurGenTec, LLC | 08/26/2026SE |
| K252184 | SOL-M Luer Lock Syringe with Exchangeable Needle TrayFMF · Traditional | Sol-Millennium Medical, Inc. | 08/25/2026SE |
| K253747 | Disposable Pen Injector (KXYC-03C02, KXYC-03A03)FMF · Traditional | Jiangsu Enjosim Medical Technology Co., Ltd. | 08/14/2026SE |
| K260208 | Ultra-Fine SAFETY Insulin SyringeFMF · Traditional | embecta Medical II, LLC | 07/13/2026SE |
| K253110 | Sol-Glide Safety Needle; Sol-Glide Safety Needle with SyringeFMF · Traditional | Sol-Millennium Medical, Inc. | 06/18/2026SE |
| K260514 | Profoject Safety Needle; Profoject Syringe with Safety Needle; Profoject Low Dead…FMF · Traditional | CMT Health PTE., Ltd. | 06/12/2026SE |
| K253112 | Sofjec (Single use Needle); Sofjec (Single use Syringe with or without Needle); Sofjec…FMF · Special | Hlb Lifescience Co., Ltd. | 05/21/2026SE |
| K252279 | Sterile Hypodermic Syringe for Single Use (20ml, 30ml, 50ml, 60ml)FMF · Traditional | Chirana T.Injecta,A.S. | 04/17/2026SE |
| K253068 | Profoject Insulin Syringes; Profoject Safelock Disposable Insulin SyringeFMF · Traditional | CMT Health PTE., Ltd. | 02/23/2026SE |
| K253769 | Instylla Delivery KitFMF · Special | Instylla, Inc. | 12/22/2025SE |
More from Instylla, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K202325 | EasyPoint Blood Collection PlusJKA · Traditional | 04/09/2021SE |
| K133635 | Easypoint NeedleFMI · Traditional | 06/17/2014SE |
| K122355 | Vanishpoint Blood Collection SetJKA · Traditional | 08/23/2013SE |
| K112512 | Vanishpoint Blood Collection SetFPA · Traditional | 10/20/2011SE |
| K081420 | Vanishpoint I.V. CatheterFOZ · Abbreviated | 11/07/2008SE |
| K072654 | Patient Safe SyringeFMF · Traditional | 12/14/2007SE |
| K051355 | Vanishpoint I.V. CatheterFOZ · Traditional | 09/23/2005SE |
| K980069 | Vanishpoint SyringeMEG · Traditional | 02/12/1998SE |
| K973301 | Anti-Stick Syringe with Integral Hypodermic Needle/Vanishpoint SyringeMEG · Traditional | 11/07/1997SE |
| K971763 | Blood Collection Tube Holder Vanishpoint Tube Holder/Small Tube AdapterFMI · Traditional | 08/26/1997SE |
Questions and answers
When was Patient Safe Luer Cap cleared by the FDA?
Patient Safe Luer Cap (K101708) received a 510(k) decision of Substantially Equivalent on February 24, 2011, 252 days after the submission was received.
What is the product code of K101708?
The FDA product code is FMF – Syringe, Piston, a Class II (moderate risk) device regulated under 21 CFR 880.5860.