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FDA 510(k)

ELECTRONIC KVP CASSETTE

K-Number: K834607 · 1984-02-21

ApplicantRadiation Measurements, Inc.
Decision Date1984-02-21
Product CodeIWN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ELECTRONIC KVP CASSETTE 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 1984-02-21 under 510(k) number K834607. The device is classified under product code IWN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRONIC KVP CASSETTE?

ELECTRONIC KVP CASSETTE is a medical device that received FDA 510(k) clearance on 1984-02-21. The listed applicant is Radiation Measurements, Inc.. The 510(k) number is K834607.

When did ELECTRONIC KVP CASSETTE receive FDA 510(k) clearance?

ELECTRONIC KVP CASSETTE received FDA 510(k) clearance on 1984-02-21, under 510(k) number K834607.

Who is the listed applicant for ELECTRONIC KVP CASSETTE?

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 ELECTRONIC KVP CASSETTE?

The FDA product code for ELECTRONIC KVP CASSETTE is IWN.

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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 DEVICEK873956ULTIMETERK873836MAMMOGRAPHIC KVP METER MODEL 232K854976RMI RESPIRATORY GATING SYSTEM MODEL 301K834483DIGI-X

View all 12 devices →

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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