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FDA 510(k)

CIRIBART GYUDUBG CATGETER

K-Number: K855103 · 1986-02-18

ApplicantMansfield Scientific, Inc.
Decision Date1986-02-18
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CIRIBART GYUDUBG CATGETER is the device name listed in this FDA 510(k) record. The listed applicant is Mansfield Scientific, Inc.. It received FDA 510(k) clearance on 1986-02-18 under 510(k) number K855103. 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 CIRIBART GYUDUBG CATGETER?

CIRIBART GYUDUBG CATGETER is a medical device that received FDA 510(k) clearance on 1986-02-18. The listed applicant is Mansfield Scientific, Inc.. The 510(k) number is K855103.

When did CIRIBART GYUDUBG CATGETER receive FDA 510(k) clearance?

CIRIBART GYUDUBG CATGETER received FDA 510(k) clearance on 1986-02-18, under 510(k) number K855103.

Who is the listed applicant for CIRIBART GYUDUBG CATGETER?

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

What is the FDA product code for CIRIBART GYUDUBG CATGETER?

The FDA product code for CIRIBART GYUDUBG CATGETER is DQO.

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Other records listing Mansfield Scientific, Inc. as applicant

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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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