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FDA 510(k)

MILLAR MIKRO-TIP DOPPLER CATHETER

K-Number: K896264 · 1990-01-24

ApplicantMillar Instruments, Inc.
Decision Date1990-01-24
Product CodeJOP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MILLAR MIKRO-TIP DOPPLER CATHETER 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 1990-01-24 under 510(k) number K896264. The device is classified under product code JOP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILLAR MIKRO-TIP DOPPLER CATHETER?

MILLAR MIKRO-TIP DOPPLER CATHETER is a medical device that received FDA 510(k) clearance on 1990-01-24. The listed applicant is Millar Instruments, Inc.. The 510(k) number is K896264.

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

MILLAR MIKRO-TIP DOPPLER CATHETER received FDA 510(k) clearance on 1990-01-24, under 510(k) number K896264.

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

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 DOPPLER CATHETER?

The FDA product code for MILLAR MIKRO-TIP DOPPLER CATHETER is JOP.

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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: JOP)

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.

K242662Falcon/Xpress (Falcon/Xpress)Viasonix , Ltd.K233976VasoGuard (V10, V8, V6, V4, V2)Corvascular Diagnostics, LLCK153762Smartdop XT6Koven Technology, Inc.K131860VASCULAB VL4000 PHOTOPLETHYSMOGRAPH WITH PULSE VOLUME RECORDINGUs Vascular, LLCK111416FALCONViasonix , Ltd.K071730STUDIODOP VICORDERSkidmore Medical, Limited

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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