Acti-Flex Arterial Extension Set
FDA 510(k) K954035 · R-Group Intl.
510(k) numberK954035
Submission
- Device name
- Acti-Flex Arterial Extension Set
- Applicant
- R-Group Intl.
Gainesville, FL, US - Received
- August 28, 1995
- Decision date
- September 25, 1995
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- CBT – Arterial Blood Sampling Kit
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 868.1100
- Specialty
- Anesthesiology
This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.
Other 510(k)s with product code CBT
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K071269 | Hemodraw Arterial Blood Sampling SystemCBT · Traditional | Smiths Medical Asd, Inc. | 08/01/2007SE |
| K070340 | Secure Arterial Blood Sampling SystemCBT · Traditional | Smiths Medical Asd, Inc. | 03/15/2007SE |
| K955663 | Abc In-Line Blood Sampling KitCBT · Traditional | Utah Medical Products, Inc. | 03/17/1997SE |
| K954015 | Abg Point Lok Needle Protection DeviceCBT · Traditional | Devon Industries, Inc. | 11/20/1995SE |
| K950098 | Needle Safety CoverCBT · Traditional | Hammer-Plane, Inc. | 08/11/1995SE |
| K945719 | Aspir-Pulse(Tm) Arterial Blood Gas (Abg) SystemCBT · Traditional | Sherwood Medical Co. | 03/16/1995SESK |
| K944941 | Piston SyringeCBT · Traditional | Martell Medical Products, Inc. | 12/05/1994SE |
| K945485 | Abg Needle ProtectionCBT · Traditional | Devon Industries, Inc. | 11/29/1994SE |
| K940575 | Aspir-Pulse(Tm) Saf-T-VentCBT · Traditional | Sherwood Medical Co. | 03/22/1994SE |
| K931873 | VacventCBT · Traditional | Steven Frank Mercereau | 12/30/1993SEKD |
More from Steven Frank Mercereau
| 510(k) | Device | Decision |
|---|---|---|
| K001233 | Acti-Flex Fluid Delivery System or Acti-Flex F D SFPA · Traditional | 12/13/2000SE |
| K001599 | Acti-Flex IV Administration SetFPA · Traditional | 09/18/2000SE |
| K993777 | Disposable and Reusable Ball and Loop ElectrodesHGI · Traditional | 05/25/2000SE |
| K952470 | Acti-Flex Low, Medium, Rescare I, Rescare Ii.GCD · Traditional | 11/28/1995SE |
| K940319 | R-Group International Coiled Low Pressure Extension LineFPA · Traditional | 11/10/1994SE |
| K913267 | R-Group Intl. One Wall Puncture NeedleDRC · Traditional | 06/05/1992SE |
Questions and answers
When was Acti-Flex Arterial Extension Set cleared by the FDA?
Acti-Flex Arterial Extension Set (K954035) received a 510(k) decision of Substantially Equivalent on September 25, 1995, 28 days after the submission was received.
What is the product code of K954035?
The FDA product code is CBT – Arterial Blood Sampling Kit, a Class I (low risk) device regulated under 21 CFR 868.1100.