CROSSLEAD Peripheral Guide Wire
FDA 510(k) K213315 · Asahi Intecc Co., Ltd.
510(k) numberK213315
Submission
- Device name
- CROSSLEAD Peripheral Guide Wire
- Applicant
- Asahi Intecc Co., Ltd.
Seto, JP - Received
- October 4, 2021
- Decision date
- July 1, 2022
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DQX – Wire, Guide, Catheter
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1330
- Specialty
- Cardiovascular
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|---|---|---|---|
| K261281 | CROSSLEAD Standard 035 and CROSSLEAD Stiff 035DQX · Traditional | Filmecc Co., Ltd. | 09/03/2026SE |
| K253667 | Accoat Guide WireDQX · Traditional | Sp Medical A/S | 07/14/2026SE |
| K261640 | Merit MAK Nitinol/Gold-Tungsten Guide WireDQX · Special | Merit Medical Ireland , Ltd. | 07/13/2026SE |
| K254137 | InQwire Amplatz Guide WireDQX · Traditional | Merit Medical Ireland, Ltd. | 05/22/2026SE |
| K260544 | FMD Peripheral Guide Wire F-14 Flex 6; FMD Peripheral Guide Wire F-14 Tapered 40; FMD…DQX · Special | FMD Co., Ltd. | 03/20/2026SE |
| K253746 | Enroute 0.014'' Transcarotid GuidewireDQX · Special | Lake Region Medical | 03/19/2026SE |
| K253262 | EmeryGlide (EG18008901)DQX · Special | Nano4imaging GmbH | 03/06/2026SE |
| K253847 | Splashwire Hydrophilic Guide Wire (MSWSTD35150J3)DQX · Special | Merit Medical Ireland, Ltd. | 01/31/2026SE |
| K251385 | InQwire Super Stiff Guide Wire (IQSS32180J3); InQwire Super Stiff Guide Wire…DQX · Traditional | Merit Medical Ireland, Ltd. | 01/21/2026SE |
| K252674 | Solo Pace Fusion System (SOLOFUSE1)DQX · Traditional | Solo Pace, Inc. | 01/09/2026SE |
More from Solo Pace, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K254178 | SAYA 86 Radial Access Guide CatheterQJP · Traditional | 05/11/2026SE |
| K252011 | CHIKAI Nexus petitMOF · Traditional | 02/02/2026SE |
| K251560 | FUBUKI XF-R Neurovascular Long SheathQJP · Special | 06/20/2025SE |
| K251240 | Branchor X Balloon Guide CatheterQJP · Traditional | 06/20/2025SE |
| K243383 | CHIKAI Nexus 014MOF · Traditional | 04/21/2025SE |
| K243733 | SION blue PLUSDQX · Special | 04/02/2025SE |
| K241962 | CrossloopDQX · Traditional | 03/27/2025SE |
| K242597 | CROSSLEAD 0.018inchDQX · Special | 03/05/2025SE |
| K241702 | CROSSLEAD 0.014inchDQX · Special | 02/06/2025SE |
| K241801 | Tornus ESFGE · Traditional | 12/17/2024SE |
Questions and answers
When was CROSSLEAD Peripheral Guide Wire cleared by the FDA?
CROSSLEAD Peripheral Guide Wire (K213315) received a 510(k) decision of Substantially Equivalent on July 1, 2022, 270 days after the submission was received.
What is the product code of K213315?
The FDA product code is DQX – Wire, Guide, Catheter, a Class II (moderate risk) device regulated under 21 CFR 870.1330.