Browse hierarchy: [Cardiovascular (CV)](/submissions/CV) → [Subpart B — Cardiovascular Diagnostic Devices](/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices) → [21 CFR 870.1300](/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/870.1300) → DQR — Cannula, Catheter # DQR · Cannula, Catheter _Cardiovascular · 21 CFR 870.1300 · Class 2_ **Canonical URL:** https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR ## Overview - **Product Code:** DQR - **Device Name:** Cannula, Catheter - **Regulation:** [21 CFR 870.1300](/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/870.1300) - **Device Class:** 2 - **Review Panel:** [Cardiovascular](/submissions/CV) - **3rd-party reviewable:** yes ## Identification A catheter cannula is a hollow tube which is inserted into a vessel or cavity; this device provides a rigid or semirigid structure which can be connected to a tube or connector. ## Classification Rationale Class II (performance standards). ## Recent Cleared Devices (20 of 25) Showing 20 most recent of 25 cleared devices. | Record | Device Name | Applicant | Decision Date | Decision | | --- | --- | --- | --- | --- | | [K131446](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K131446.md) | INTEGRA JARIT HEPARIN CANNULAS, INJECTORS, AND NEEDLES | Integra LifeSciences Corporation | Oct 28, 2013 | SESE | | [K073559](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K073559.md) | 18 FR. RMI ARTERIAL PERFUSION CANNULA II, 20 FR. RMI ARTERIAL PERFUSION CANNULA II | Edwards Lifesciences Research Medical | Jan 31, 2008 | SESE | | [K051655](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K051655.md) | ANGIODYNAMICS, INC., MICRO ACCESS KITS | AngioDynamics, Inc. | Sep 12, 2005 | SESE | | [K030398](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K030398.md) | CARDIACASSIST TRANSSEPTAL CANNULA SET, MODEL 5132-6221 | Cardiacassist, Inc. | May 23, 2003 | SESE | | [K960098](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K960098.md) | RMI INTERNAL MAMMARY ARTERY CANNULA | Research Medical, Inc. | Mar 26, 1996 | SESE | | [K902674](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K902674.md) | DATASCOPE ARTERIAL CANNULA W/ACCESS PORT | Datascope Corp. | Jan 16, 1991 | SESE | | [K894784](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K894784.md) | MODIFIED SHILEY FEMORAL VENOUS CANNULA | Shiley, Inc. | Mar 28, 1990 | SESE | | [K894243](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K894243.md) | RMI ARTERIAL PERFUSION CANNULA | Research Medical, Inc. | Sep 19, 1989 | SESE | | [K884628](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K884628.md) | HARBORIN CENTRAL VENOUS CATHETER | Harbor Medical Devices, Inc. | May 15, 1989 | SESE | | [K884478](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K884478.md) | DAIG COLLAPSIBLE STERILE SLEEVE | Daig Corp. | Feb 22, 1989 | SESE | | [K884375](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K884375.md) | TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER | Argon Medical Corp. | Jan 11, 1989 | SESE | | [K882977](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K882977.md) | ASK-300 | Medical Repackers Co. | Jan 5, 1989 | SESE | | [K881884](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K881884.md) | HARBOR CENTRAL VENOUS CATHETER | Harbor Medical Devices, Inc. | Jul 28, 1988 | SESE | | [K880771](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K880771.md) | MEDSURG 7 FR. DUAL LUMEN CENTRAL VEIN CATH SYSTEM | Medsurg Industries, Inc. | May 3, 1988 | SESE | | [K880776](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K880776.md) | 7 FR. TRIPLE LUMEN CENTRAL VEIN CATHETERI. SYSTEM | Medsurg Industries, Inc. | May 2, 1988 | SESE | | [K873012](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K873012.md) | INFANT CANNULA | Gresco International, Inc. | May 2, 1988 | SESE | | [K874618](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K874618.md) | BAXTER ACCUPORT(TM) CENTRAL VENOUS CATHETER | Bentley Laboratories, Inc. | Jan 19, 1988 | SESE | | [K872983](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K872983.md) | TORAY ANTHRON ANGIOGRAPHIC CATHETERS | Toray Industries (America), Inc. | Nov 20, 1987 | SESE | | [K870826](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K870826.md) | ADDITIONAL LETTER DESIGNATION FOR AORTIC ARCH CAN. | Shiley, Inc. | Mar 23, 1987 | SESE | | [K870825](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR/K870825.md) | NEW MODEL STYLES FOR AORTIC ARCH CANNULA | Shiley, Inc. | Mar 23, 1987 | SESE | ## Top Applicants - Shiley, Inc. — 3 clearances - Harbor Medical Devices, Inc. — 2 clearances - Medsurg Industries, Inc. — 2 clearances - Research Medical, Inc. — 2 clearances - AngioDynamics, Inc. — 1 clearance --- **Source:** [https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQR) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. 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