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FDA 510(k)

TRANSLUCENT POLY. CATH. CONNECTOR AND

K-Number: K830237 · 1983-02-18

ApplicantVertex Medical Corp.
Decision Date1983-02-18
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TRANSLUCENT POLY. CATH. CONNECTOR AND is the device name listed in this FDA 510(k) record. The listed applicant is Vertex Medical Corp.. It received FDA 510(k) clearance on 1983-02-18 under 510(k) number K830237. 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 TRANSLUCENT POLY. CATH. CONNECTOR AND?

TRANSLUCENT POLY. CATH. CONNECTOR AND is a medical device that received FDA 510(k) clearance on 1983-02-18. The listed applicant is Vertex Medical Corp.. The 510(k) number is K830237.

When did TRANSLUCENT POLY. CATH. CONNECTOR AND receive FDA 510(k) clearance?

TRANSLUCENT POLY. CATH. CONNECTOR AND received FDA 510(k) clearance on 1983-02-18, under 510(k) number K830237.

Who is the listed applicant for TRANSLUCENT POLY. CATH. CONNECTOR AND?

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

What is the FDA product code for TRANSLUCENT POLY. CATH. CONNECTOR AND?

The FDA product code for TRANSLUCENT POLY. CATH. CONNECTOR AND is DQO.

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Other records listing Vertex Medical Corp. as applicant

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Related Devices (Code: DQO)

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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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