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FDA 510(k)

ACIST ANGIOGRAPHIC INJECTION SYSTEM, MODEL R2000-CMS

K-Number: K010390 · 2001-03-09

ApplicantAcist Medical Systems, Inc.
Decision Date2001-03-09
Product CodeDXT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ACIST ANGIOGRAPHIC INJECTION SYSTEM, MODEL R2000-CMS is the device name listed in this FDA 510(k) record. The listed applicant is Acist Medical Systems, Inc.. It received FDA 510(k) clearance on 2001-03-09 under 510(k) number K010390. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACIST ANGIOGRAPHIC INJECTION SYSTEM, MODEL R2000-CMS?

ACIST ANGIOGRAPHIC INJECTION SYSTEM, MODEL R2000-CMS is a medical device that received FDA 510(k) clearance on 2001-03-09. The listed applicant is Acist Medical Systems, Inc.. The 510(k) number is K010390.

When did ACIST ANGIOGRAPHIC INJECTION SYSTEM, MODEL R2000-CMS receive FDA 510(k) clearance?

ACIST ANGIOGRAPHIC INJECTION SYSTEM, MODEL R2000-CMS received FDA 510(k) clearance on 2001-03-09, under 510(k) number K010390.

Who is the listed applicant for ACIST ANGIOGRAPHIC INJECTION SYSTEM, MODEL R2000-CMS?

The FDA 510(k) record lists Acist Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACIST ANGIOGRAPHIC INJECTION SYSTEM, MODEL R2000-CMS?

The FDA product code for ACIST ANGIOGRAPHIC INJECTION SYSTEM, MODEL R2000-CMS is DXT.

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Other records listing Acist Medical Systems, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262115VueJect® Ultrasound Enhancing Agent Delivery SystemK252638VeraPro S100 Multi-Use Syringe (018808); VeraPro S100 LV1 Low Viscosity Single-Use Syringe (018811); VeraPro AMT Auto-Manifold and Transducer (018814); VeraPro AngioTouch FLX165 Hand Controller Kit (018806); VeraPro AngioTouch HiFi165 Hand Controller Kit (018804)K252653ACIST Pro Diagnostic System (019304); Processing Unit Bed Mount; AngioTouch Module; ACIST Pro Cart; Single Transducer Cable; Triple Transducer CableK233904ACIST RXi System (016616); ACIST Navvus II Catheter (016675_K203004ACIST CVi1 Contrast Delivery System, ACIST CVi Contrast Delivery SystemK193183ACIST HDi System, ACIST Kodama Intravascular Ultrasound Catheter

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Related Devices (Code: DXT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252652Disposable Syringes with Accessories for Power Injectors (900103T); Disposable Syringes with Accessories for Power Injectors (900103H); Disposable Syringes with Accessories for Power Injectors (801800H); Disposable Syringes with Accessories for Power Injectors (800099T); Disposable Syringes with Accessories for Power Injectors (800099H); Disposable Syringes with Accessories for Power Injectors (800096T); Disposable Syringes with Accessories for Power Injectors (800096H); Disposable SyrFortis Biosolutions Company LimitedK252653ACIST Pro Diagnostic System (019304); Processing Unit Bed Mount; AngioTouch Module; ACIST Pro Cart; Single Transducer Cable; Triple Transducer CableAcist Medical Systems, Inc.K252638VeraPro S100 Multi-Use Syringe (018808); VeraPro S100 LV1 Low Viscosity Single-Use Syringe (018811); VeraPro AMT Auto-Manifold and Transducer (018814); VeraPro AngioTouch FLX165 Hand Controller Kit (018806); VeraPro AngioTouch HiFi165 Hand Controller Kit (018804)Acist Medical Systems, Inc.K253048High Pressure Syringe; Pressure Connecting Tube; Quick fill tube; Spike; Transfer TubeShenzhen Maiwei Biotech Co., Ltd.K251788Extension tubeZhuhai DR Medical Instruments Co., Ltd.K252891MEDRAD MRXperion MR Injection System and MR Injection System Syringe Kit; MEDRAD ISI2 Module (ISI2)Bayer Medical Care, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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