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FDA 510(k)

MAMMOGRAPHIC KVP METER MODEL 232

K-Number: K873836 · 1987-10-16

ApplicantRadiation Measurements, Inc.
Decision Date1987-10-16
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAMMOGRAPHIC KVP METER MODEL 232 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 1987-10-16 under 510(k) number K873836. The device is classified under product code IZH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAMMOGRAPHIC KVP METER MODEL 232?

MAMMOGRAPHIC KVP METER MODEL 232 is a medical device that received FDA 510(k) clearance on 1987-10-16. The listed applicant is Radiation Measurements, Inc.. The 510(k) number is K873836.

When did MAMMOGRAPHIC KVP METER MODEL 232 receive FDA 510(k) clearance?

MAMMOGRAPHIC KVP METER MODEL 232 received FDA 510(k) clearance on 1987-10-16, under 510(k) number K873836.

Who is the listed applicant for MAMMOGRAPHIC KVP METER MODEL 232?

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 MAMMOGRAPHIC KVP METER MODEL 232?

The FDA product code for MAMMOGRAPHIC KVP METER MODEL 232 is IZH.

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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.

K893216RMI ULTRASOUND DOPPLER PHANTOM SYSTEMK885223RMI SHORT DISTANCE ALIGNMENT DEVICEK873956ULTIMETERK854976RMI RESPIRATORY GATING SYSTEM MODEL 301K834483DIGI-XK834607ELECTRONIC KVP CASSETTE

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Related Devices (Code: IZH)

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.

K203509SMART FINDERIms Giotto S.P.A.K202294Affirm Contrast BiopsyHologic, Inc.K191495Biopsy PositionerFujifilm CorporationK161575Affirm Lateral Arm Upright Biopsy AccessoryHologicK161920Comfort CoverPrecision Dynamics CorporationK153486Affirm Prone Biopsy SystemHologic, 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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