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FDA 510(k)

RMI TRANSILLUMINATOR, MODEL 292

K-Number: K812949 · 1981-12-02

ApplicantRadiation Measurements, Inc.
Decision Date1981-12-02
Product CodeHJM
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RMI TRANSILLUMINATOR, MODEL 292 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 1981-12-02 under 510(k) number K812949. The device is classified under product code HJM. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RMI TRANSILLUMINATOR, MODEL 292?

RMI TRANSILLUMINATOR, MODEL 292 is a medical device that received FDA 510(k) clearance on 1981-12-02. The listed applicant is Radiation Measurements, Inc.. The 510(k) number is K812949.

When did RMI TRANSILLUMINATOR, MODEL 292 receive FDA 510(k) clearance?

RMI TRANSILLUMINATOR, MODEL 292 received FDA 510(k) clearance on 1981-12-02, under 510(k) number K812949.

Who is the listed applicant for RMI TRANSILLUMINATOR, MODEL 292?

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 TRANSILLUMINATOR, MODEL 292?

The FDA product code for RMI TRANSILLUMINATOR, MODEL 292 is HJM.

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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

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Related Devices (Code: HJM)

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.

K972506INFINITECH BULLET ENDO ILLUMINATED PICK MANIPULATORInfinitech, Inc.K950529PEREGRINE DIFFUSION LIGHT PIPEPeregrine Surgical , Ltd.K945877WECO ENDOSCOPIC SYSTEMS WITH FIBER OPTIC LIGHTWells Johnson Co.K931072HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBEHgm, Inc.K933445DPS 100 MULTIPORT ILLUMINATION SYSTEM (MIS)Storz Instrument Co.K940393PEREGRINE WIDE ANGLE LIGHT PIPEPeregrine Surgical , Ltd.

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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