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FDA 510(k)

ULTIMETER

K-Number: K873956 · 1987-10-30

ApplicantRadiation Measurements, Inc.
Decision Date1987-10-30
Product CodeLHO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ULTIMETER 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 1987-10-30 under 510(k) number K873956. The device is classified under product code LHO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTIMETER?

ULTIMETER is a medical device that received FDA 510(k) clearance on 1987-10-30. The listed applicant is Radiation Measurements, Inc.. The 510(k) number is K873956.

When did ULTIMETER receive FDA 510(k) clearance?

ULTIMETER received FDA 510(k) clearance on 1987-10-30, under 510(k) number K873956.

Who is the listed applicant for ULTIMETER?

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 ULTIMETER?

The FDA product code for ULTIMETER is LHO.

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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 DEVICEK873836MAMMOGRAPHIC KVP METER MODEL 232K854976RMI RESPIRATORY GATING SYSTEM MODEL 301K834483DIGI-XK834607ELECTRONIC KVP CASSETTE

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Related Devices (Code: LHO)

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.

K042733STANDARD IMAGING PIPSPRO QA SOFTWARE SYSTEMStandard Imaging, Inc.K853754MAGNETIC RESONANCE IMAGING UNIFORMITY/T1 76-901Victoreen, Inc.K860260MULTI PURPOSE MODEL 76-903Victoreen, Inc.K860100MRI SLICE THICKNESS & CONTIGUITY PHANTOM #76-902Victoreen, Inc.K844620BDS-3 BEAM DATA SCANNERVarian Assoc., Inc.K845007RFA-7 RADIATION FIELD ANALYZERVarian Assoc., 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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