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FDA 510(k)

MIKRO-TIP CATHETER PRESSURE TRANSDUCER

K-Number: K823434 · 1982-11-30

ApplicantMillar Instruments, Inc.
Decision Date1982-11-30
Product CodeDRF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

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 1982-11-30 under 510(k) number K823434. The device is classified under product code DRF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIKRO-TIP CATHETER PRESSURE TRANSDUCER?

MIKRO-TIP CATHETER PRESSURE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1982-11-30. The listed applicant is Millar Instruments, Inc.. The 510(k) number is K823434.

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

MIKRO-TIP CATHETER PRESSURE TRANSDUCER received FDA 510(k) clearance on 1982-11-30, under 510(k) number K823434.

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

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

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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: DRF)

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.

K252794Vision-MR™ Diagnostic CatheterImricor Medical Systems, Inc.K250590MAGiC Sweep™ EP Mapping CatheterStereotaxis, Inc.K250310VIKING™ Fixed Curve Diagnostic CatheterBoston Scientific CorporationK240366EP•XT™ Unidirectional Steerable Diagnostic Catheter; Dynamic Tip™ Unidirectional Steerable Diagnostic Catheter; Dynamic XT™ Unidirectional Steerable Diagnostic CatheterBoston Scientific CorporationK233900Nordica PV Cryo Mapping CatheterSynaptic Medical CorporationK233397Cosine-10TM Diagnostic CatheterMedtronic, 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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