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FDA 510(k)

X-RAY MONOBLOCK, MONOBLOCK XRS-60-330

K-Number: K000052 · 2000-02-10

ApplicantDynarad Corp.
Decision Date2000-02-10
Product CodeITY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

X-RAY MONOBLOCK, MONOBLOCK XRS-60-330 is the device name listed in this FDA 510(k) record. The listed applicant is Dynarad Corp.. It received FDA 510(k) clearance on 2000-02-10 under 510(k) number K000052. The device is classified under product code ITY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-RAY MONOBLOCK, MONOBLOCK XRS-60-330?

X-RAY MONOBLOCK, MONOBLOCK XRS-60-330 is a medical device that received FDA 510(k) clearance on 2000-02-10. The listed applicant is Dynarad Corp.. The 510(k) number is K000052.

When did X-RAY MONOBLOCK, MONOBLOCK XRS-60-330 receive FDA 510(k) clearance?

X-RAY MONOBLOCK, MONOBLOCK XRS-60-330 received FDA 510(k) clearance on 2000-02-10, under 510(k) number K000052.

Who is the listed applicant for X-RAY MONOBLOCK, MONOBLOCK XRS-60-330?

The FDA 510(k) record lists Dynarad Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for X-RAY MONOBLOCK, MONOBLOCK XRS-60-330?

The FDA product code for X-RAY MONOBLOCK, MONOBLOCK XRS-60-330 is ITY.

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Other records listing Dynarad Corp. as applicant

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K981267FACTS MONOBLOCKK973833CONTROL, X-RAY DIAGNOSTIC, GENERATOR, HIGH VOLTAGE, ASSEMBLY, TUBE HOUSING DIAGNOSTIC, BEAM LIMITING DEVICE, MANUALK932356NOVA XM2K941363PHANTOMK932353HF-110AK9323559150A, 1100F

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Related Devices (Code: ITY)

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.

K933162MRX-750Mrx Corp.K923094MOLYBDENUMSoutheastern Medical Diagnostics, Inc.K923141PHILIPS PRE-FILTER OPTIONPhilips Medical Systems, Inc.K921129MRX-700Mrx-Ray Tube Corp.K921130MRX-865Mrx-Ray Tube Corp.K921316MG-1001 TUBE HOUSING ASSEMBLYMagma Corp.

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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