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)

NAMIC ADB ANGIOGRAPHIC DUMP BAG

K-Number: K843726 · 1984-10-18

ApplicantNorth American Instrument Corp.
Decision Date1984-10-18
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NAMIC ADB ANGIOGRAPHIC DUMP BAG is the device name listed in this FDA 510(k) record. The listed applicant is North American Instrument Corp.. It received FDA 510(k) clearance on 1984-10-18 under 510(k) number K843726. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAMIC ADB ANGIOGRAPHIC DUMP BAG?

NAMIC ADB ANGIOGRAPHIC DUMP BAG is a medical device that received FDA 510(k) clearance on 1984-10-18. The listed applicant is North American Instrument Corp.. The 510(k) number is K843726.

When did NAMIC ADB ANGIOGRAPHIC DUMP BAG receive FDA 510(k) clearance?

NAMIC ADB ANGIOGRAPHIC DUMP BAG received FDA 510(k) clearance on 1984-10-18, under 510(k) number K843726.

Who is the listed applicant for NAMIC ADB ANGIOGRAPHIC DUMP BAG?

The FDA 510(k) record lists North American Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NAMIC ADB ANGIOGRAPHIC DUMP BAG?

The FDA product code for NAMIC ADB ANGIOGRAPHIC DUMP BAG is DQO.

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 North American Instrument Corp. 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.

K960801SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS)K955554HEMO-VALVEK960310EPIC INTRODUCER SHEATHK922552MORSE(R) ANGIOGRAPHIC CATHETERSK915078MORSE HEMOSTATIC CATHETER INTRODUCER SETK905208MORSE ANESTHESIA

View all 28 devices →

Related Devices (Code: DQO)

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.

K261455Arterial Pressure Monitoring Set/TraySpectrum VascularK252702Bioptimal Pulmonary Artery Monitoring Catheter (TD2502NF, TD2502NGF, TD2502NDF, TD2502NCF, TD2502NCGF, TD2502NDGF, TD2502NDCF, TD2502NDCGF, TD2502NXCF, TD2502NDXF, TD2502NXCGF, TD2502NDXGF, TD2502NDXCF, TD2502NDXCGF, TD2502-110NF, TD2502-110NGF, TD2502-110NDF, TD2502-110NCF, TD2502-110NDGF, TD2502-110NDCF, TD2502-110NCGF, TD2502-110NDCGF, TD2502-110NXF, TD2502-110NXGF, TD2502-110NDXF, TD2502-110NXCF, TD2502-110NDXGF, TD2502-110NDXCF ,TD2502-110NXCGF, TD2502-110NDXCGF, TD2602NF, TD2602NBioptimal International Pte. , Ltd.K254278Arterial Pressure Monitoring Set/TraySpectrum VascularK250751DualView CatheterTerumo CorporationK242966Gentuity® HF-OCT Imaging System with Vis-Rx Prime® Micro-Imaging CatheterGentuity, LLCK242420pNOVUS 21 MicrocatheterPhenox, Ltd.

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.

↑