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FDA 510(k)

MILLAR MIKRO-TIP PULSE TRANSDUCER

K-Number: K895721 · 1989-12-07

ApplicantMillar Instruments, Inc.
Decision Date1989-12-07
Product CodeDXO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MILLAR MIKRO-TIP PULSE 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 1989-12-07 under 510(k) number K895721. The device is classified under product code DXO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILLAR MIKRO-TIP PULSE TRANSDUCER?

MILLAR MIKRO-TIP PULSE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1989-12-07. The listed applicant is Millar Instruments, Inc.. The 510(k) number is K895721.

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

MILLAR MIKRO-TIP PULSE TRANSDUCER received FDA 510(k) clearance on 1989-12-07, under 510(k) number K895721.

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

The FDA product code for MILLAR MIKRO-TIP PULSE TRANSDUCER is DXO.

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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: DXO)

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.

K251367OptoMonitor 3Opsens, Inc.K241418OptoMonitor 3Opsens, Inc.K233904ACIST RXi System (016616); ACIST Navvus II Catheter (016675_Acist Medical Systems, Inc.K222216TruWave Disposable Pressure TransducerEdwards Lifesciences, LLCK202943OptoMonitor 3Opsens, Inc.K193620OptoMonitor 3Opsens, Inc.

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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