Valvulotome
FDA 510(k) K925283 · Intramed Laboratories, Inc.
510(k) numberK925283
Submission
- Device name
- Valvulotome
- Applicant
- Intramed Laboratories, Inc.
San Diego, CA, US - Received
- October 20, 1992
- Decision date
- February 10, 1994
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MGZ – Valvulotome
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.4885
- Specialty
- Cardiovascular
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|---|---|---|---|
| K260188 | LimFlow VectorMGZ · Special | LimFlow, Inc. | 03/18/2026SE |
| K250105 | Boomerang Valvulotome (BMGVT080); Boomerang Push Valvulotome (BMGPVT125)MGZ · Traditional | Aveera Medical, Inc. | 07/03/2025SE |
| K221902 | LimFlow VectorMGZ · Traditional | LimFlow, Inc. | 12/21/2022SE |
| K190267 | EZE SIT ValvulotomeMGZ · Traditional | Lemaitre Vascular | 10/30/2019SE |
| K142660 | Antegrade LeMills ValvulotomeMGZ · Special | LeMaitre Vascular, Inc. | 10/17/2014SE |
| K140042 | 1.5MM Hydro Expandable Lemaitre ValvulotomeMGZ · Traditional | LeMaitre Vascular, Inc. | 04/10/2014SE |
| K132047 | Lemills ValvulotomeMGZ · Traditional | LeMaitre Vascular, Inc. | 11/05/2013SE |
| K132190 | Expandable Lemaitre Valvulotome, Over-The-Wire Lemaitre ValvulotomeMGZ · Traditional | LeMaitre Vascular, Inc. | 08/05/2013SE |
| K111884 | Over-The-Wire Expandable Lemaitre ValvulotomeMGZ · Special | LeMaitre Vascular, Inc. | 07/29/2011SE |
| K080178 | Valvulotome by KovenMGZ · Traditional | Koven Technology, Inc. | 07/28/2008SE |
More from Koven Technology, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K953258 | Titanium Hemostatic ClipFZP · Traditional | 01/05/1996SE |
| K942457 | Graft Thrombectomy InstrumentsMCW · Traditional | 02/07/1995SE |
| K931792 | ArthroscopeHRH · Traditional | 06/13/1994SE |
| K934696 | AngioscopeLYK · Traditional | 01/18/1994SE |
| K922114 | Endoscopic Retrieval BasketFFL · Traditional | 08/03/1992SE |
| K914385 | Optical ValvulotomeMGZ · Traditional | 03/02/1992SE |
| K904465 | Flexible ArthroscopeHRX · Traditional | 12/20/1990SE |
| K903528 | LaparoscopeHET · Traditional | 09/04/1990SE |
| K902444 | Clearview(Tm) Angioscopic Irrigation PumpDQI · Traditional | 08/30/1990SE |
| K901010 | Flexible CholedochoscopeFBN · Traditional | 05/22/1990SE |
Questions and answers
When was Valvulotome cleared by the FDA?
Valvulotome (K925283) received a 510(k) decision of Substantially Equivalent on February 10, 1994, 478 days after the submission was received.
What is the product code of K925283?
The FDA product code is MGZ – Valvulotome, a Class II (moderate risk) device regulated under 21 CFR 870.4885.