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FDA 510(k)

RMI ULTRASOUND DOPPLER PHANTOM SYSTEM

K-Number: K893216 · 1989-09-05

ApplicantRadiation Measurements, Inc.
Decision Date1989-09-05
Product CodeGXX
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

RMI ULTRASOUND DOPPLER PHANTOM SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Radiation Measurements, Inc.. It received FDA 510(k) clearance on 1989-09-05 under 510(k) number K893216. The device is classified under product code GXX. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RMI ULTRASOUND DOPPLER PHANTOM SYSTEM?

RMI ULTRASOUND DOPPLER PHANTOM SYSTEM is a medical device that received FDA 510(k) clearance on 1989-09-05. The listed applicant is Radiation Measurements, Inc.. The 510(k) number is K893216.

When did RMI ULTRASOUND DOPPLER PHANTOM SYSTEM receive FDA 510(k) clearance?

RMI ULTRASOUND DOPPLER PHANTOM SYSTEM received FDA 510(k) clearance on 1989-09-05, under 510(k) number K893216.

Who is the listed applicant for RMI ULTRASOUND DOPPLER PHANTOM SYSTEM?

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

What is the FDA product code for RMI ULTRASOUND DOPPLER PHANTOM SYSTEM?

The FDA product code for RMI ULTRASOUND DOPPLER PHANTOM SYSTEM is GXX.

Related Clinical Trials

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Other records listing Radiation Measurements, 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.

K885223RMI SHORT DISTANCE ALIGNMENT DEVICEK873956ULTIMETERK873836MAMMOGRAPHIC KVP METER MODEL 232K854976RMI RESPIRATORY GATING SYSTEM MODEL 301K834483DIGI-XK834607ELECTRONIC KVP CASSETTE

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Related Devices (Code: GXX)

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.

K844247ULTRASONIC SCANNER CALIBRATION & TEST PHANTOMSTechnicare Corp.K844120ULTRASONIC SCANNER CALIBRATION & TEST OBJECTSEcho Ultrasound

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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