Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAY

K-Number: K955689 · 1996-05-15

ApplicantContour Fabricators of Florida, Inc.
Decision Date1996-05-15
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Contour Fabricators of Florida, Inc.. It received FDA 510(k) clearance on 1996-05-15 under 510(k) number K955689. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAY?

RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAY is a medical device that received FDA 510(k) clearance on 1996-05-15. The listed applicant is Contour Fabricators of Florida, Inc.. The 510(k) number is K955689.

When did RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAY receive FDA 510(k) clearance?

RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAY received FDA 510(k) clearance on 1996-05-15, under 510(k) number K955689.

Who is the listed applicant for RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAY?

The FDA 510(k) record lists Contour Fabricators of Florida, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAY?

The FDA product code for RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAY is DWS.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Contour Fabricators of Florida, 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.

K955685RNS STERILE, DISPOSABLE CT BIOPSY TRAYK962040RNS ARTHROGRAM TRAYK955687RNS STERILE, DISPOSABLE RADIOGRAPHIC CONTRAST TRAYK955684RNS STERILE, DISPOSABLE ANGIOGRAPHIC TRAYK955679RNS STERILE, DISPOSABLE AMNIOCENTESIS TRAYK955686RNS, STERILE DISPOSABLE PERCUTANEOUS CHOLANGIOGRAPHIC TRAY

View all 18 devices →

Related Devices (Code: DWS)

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.

K022238MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626Medtronic VascularK964445OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006)Dlp, Inc.K962771BURKE CONGENITAL THORACOSCOPY INSTRUMENTSPilling Weck, Inc.K960139G.E. STERILE ANGIOGRAPHIC TRAYGE Medical SystemsK960144G.E. STERILE CT BIOPSY TRAYGE Medical SystemsK960143G.E. STERILE DIGITAL ANGIOGRAPHIC TRAYGE Medical Systems

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.

↑