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FDA 510(k)

MILLAR MIKRO-TIP CATHETER PRESSURE TRANSDUCER

K-Number: K883651 · 1988-11-18

ApplicantMillar Instruments, Inc.
Decision Date1988-11-18
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MILLAR MIKRO-TIP CATHETER PRESSURE TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Millar Instruments, Inc.. It received FDA 510(k) clearance on 1988-11-18 under 510(k) number K883651. 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 MILLAR MIKRO-TIP CATHETER PRESSURE TRANSDUCER?

MILLAR MIKRO-TIP CATHETER PRESSURE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1988-11-18. The listed applicant is Millar Instruments, Inc.. The 510(k) number is K883651.

When did MILLAR MIKRO-TIP CATHETER PRESSURE TRANSDUCER receive FDA 510(k) clearance?

MILLAR MIKRO-TIP CATHETER PRESSURE TRANSDUCER received FDA 510(k) clearance on 1988-11-18, under 510(k) number K883651.

Who is the listed applicant for MILLAR MIKRO-TIP CATHETER PRESSURE TRANSDUCER?

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

What is the FDA product code for MILLAR MIKRO-TIP CATHETER PRESSURE TRANSDUCER?

The FDA product code for MILLAR MIKRO-TIP CATHETER PRESSURE TRANSDUCER is DQO.

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Other records listing Millar Instruments, 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.

K112323CARDIA-CATHK093111MIKRO-CATH, MODEL 825-0101K013205MILLAR PRESSURE CONTROL UNIT MODEL PCU-2000K993694MIKRO-TIP ANGIOGRAPHIC CATHETERK952773MIKRO-TIP ANGIOGRAPHIC CATHETERK935166FLOW DIRECTED MIKRO-TIP PRESSURE TRANSDUCER

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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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