Timleine(Tm) Venipuncture System
FDA 510(k) K870770 · Ipax, Inc.
510(k) numberK870770
Submission
- Device name
- Timleine(Tm) Venipuncture System
- Applicant
- Ipax, Inc.
Englewood, CO, US - Received
- February 26, 1987
- Decision date
- April 23, 1987
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- KMK – Device, Intravascular Catheter Securement
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 880.5210
- Specialty
- General Hospital
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|---|---|---|---|
| K180994 | SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath…KMK · Traditional | Interrad Medical, Inc. | 07/09/2019SE |
| K981860 | A P HarnessKMK · Traditional | Paraworks Enterprise, Ltd. | 06/03/1999SE |
| K963365 | Multi-Purpose Medical Tube HolderKMK · Traditional | Byrd Medical Devices, Inc. | 10/11/1996SE |
| K941098 | Secure-SiteKMK · Traditional | Op-Co Medical Products , Ltd. | 08/09/1995SE |
| K943147 | Statlock CVKMK · Traditional | Venetec, Inc. | 09/29/1994SE |
| K943047 | IV Start KitsKMK · Traditional | Sterile Concepts, Inc. | 09/14/1994SE |
| K941940 | Immobile Sterile and Immobile A/C SterileKMK · Traditional | Tnt Moborg Intl. , Ltd. | 07/14/1994SE |
| K941850 | Immobile Non-Sterile and Immobile A/C Non-SterileKMK · Traditional | Tnt Moborg Intl. , Ltd. | 07/14/1994SE |
| K935389 | Conmed Veni-Gard I.V. DressingKMK · Traditional | Conmedcorp | 03/07/1994SE |
| K935252 | K-Lok Catheter Securement Device ModificationKMK · Traditional | K-Lok, Inc. | 02/18/1994SE |
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| K200893 | ProntoPump Sterile Tube SetLHI · Traditional | 05/04/2021SE |
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| K971245 | Blink External Eyelid WeightMML · Traditional | 06/20/1997SE |
| K915158 | Surebreath Dome, E-Z BreatherGAD · Traditional | 02/12/1992SE |
| K915118 | Phaco Emulsification,Irrigation/Aspiration TubeHQC · Traditional | 12/27/1991SE |
| K914221 | Kpe 220 TS, NonsterileHQE · Traditional | 10/25/1991SE |
| K914172 | Kpe 230 AmHQC · Traditional | 10/25/1991SE |
| K884076 | Surebreath DomeGAD · Traditional | 10/07/1988SE |
| K873097 | Procedual Changes/Assembly Process for Plus PaksGBQ · Traditional | 09/04/1987SE |
| K864726 | I/A/Kpe TipHQC · Traditional | 01/20/1987SE |
Questions and answers
When was Timleine(Tm) Venipuncture System cleared by the FDA?
Timleine(Tm) Venipuncture System (K870770) received a 510(k) decision of Substantially Equivalent on April 23, 1987, 56 days after the submission was received.
What is the product code of K870770?
The FDA product code is KMK – Device, Intravascular Catheter Securement, a Class I (low risk) device regulated under 21 CFR 880.5210.