Percuglide
FDA 510(k) K960917 · Scientific Device Manufacturer, LLC
510(k) numberK960917
Submission
- Device name
- Percuglide
- Applicant
- Scientific Device Manufacturer, LLC
San Rafael, CA, US - Received
- March 6, 1996
- Decision date
- July 2, 1996
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DRE – Dilator, Vessel, For Percutaneous Catheterization
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1310
- Specialty
- Cardiovascular
Other 510(k)s with product code DRE
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261310 | FlexTract Deflectable-Rotational Dilator Sheath SetDRE · Traditional | Merit Medical Systems, Inc. | 07/27/2026SE |
| K253616 | ProtekDilate Vascular Access KitDRE · Special | Sorin Group Italia S.R.L. | 12/19/2025SE |
| K251325 | VersaCross Connect Transseptal DilatorDRE · Special | Baylis Medical Company, Inc. | 05/29/2025SE |
| K242229 | Micro Ace Gold Advanced Micro Access SystemDRE · Traditional | Merit Medical Systems, Inc. | 01/15/2025SE |
| K241720 | VersaCross Connect Transseptal DilatorDRE · Special | Baylis Medical Company, Inc. | 07/12/2024SE |
| K233647 | VersaCross Connect Transseptal DilatorDRE · Special | Baylis Medical Company, Inc. | 12/14/2023SE |
| K232609 | Micro Ace Advanced Micro Access SystemDRE · Special | Merit Medical Systems, Inc. | 09/27/2023SE |
| K223472 | TightRail Guardian Motorized Dilator Sheath, 9 French (575-009); TightRail Guardian…DRE · Special | Spectranetics, Inc. | 12/15/2022SE |
| K212784 | TightRail Guardian Motorized Dilator SheathDRE · Traditional | Spectranetics, Inc. | 08/24/2022SE |
| K211679 | Xtractor deviceDRE · Traditional | Xcardia Innovation , Ltd. | 02/17/2022SE |
More from Xcardia Innovation , Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K960764 | Safe-CathFOZ · Traditional | 04/24/1997SE |
| K960431 | Pressure Stopcock/ManifoldFPA · Traditional | 10/29/1996SE |
| K961290 | Iup - Tip Trans, Iup - Proxi TransKXO · Traditional | 10/15/1996SE |
| K960430 | Control SyringeDXT · Traditional | 08/06/1996SE |
| K952579 | Toco TransducerHFM · Traditional | 08/04/1995SE |
Questions and answers
When was Percuglide cleared by the FDA?
Percuglide (K960917) received a 510(k) decision of Substantially Equivalent on July 2, 1996, 118 days after the submission was received.
What is the product code of K960917?
The FDA product code is DRE – Dilator, Vessel, For Percutaneous Catheterization, a Class II (moderate risk) device regulated under 21 CFR 870.1310.