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FDA 510(k)

MORSE(R) ANGIOGRAPHIC CATHETERS

K-Number: K922552 · 1993-03-03

ApplicantNorth American Instrument Corp.
Decision Date1993-03-03
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MORSE(R) ANGIOGRAPHIC CATHETERS 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 1993-03-03 under 510(k) number K922552. 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 MORSE(R) ANGIOGRAPHIC CATHETERS?

MORSE(R) ANGIOGRAPHIC CATHETERS is a medical device that received FDA 510(k) clearance on 1993-03-03. The listed applicant is North American Instrument Corp.. The 510(k) number is K922552.

When did MORSE(R) ANGIOGRAPHIC CATHETERS receive FDA 510(k) clearance?

MORSE(R) ANGIOGRAPHIC CATHETERS received FDA 510(k) clearance on 1993-03-03, under 510(k) number K922552.

Who is the listed applicant for MORSE(R) ANGIOGRAPHIC CATHETERS?

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 MORSE(R) ANGIOGRAPHIC CATHETERS?

The FDA product code for MORSE(R) ANGIOGRAPHIC CATHETERS is DQO.

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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.

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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 SHEATHK915078MORSE HEMOSTATIC CATHETER INTRODUCER SETK905208MORSE ANESTHESIAK912961MORSE VASCULAR INTRODUCER SET

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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.

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