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FDA 510(k)

X-RAY TUBE, ROTATING ANODE

K-Number: K770336 · 1977-03-01

ApplicantLitton Medical Systems
Decision Date1977-03-01
Product CodeITY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

X-RAY TUBE, ROTATING ANODE is the device name listed in this FDA 510(k) record. The listed applicant is Litton Medical Systems. It received FDA 510(k) clearance on 1977-03-01 under 510(k) number K770336. 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 TUBE, ROTATING ANODE?

X-RAY TUBE, ROTATING ANODE is a medical device that received FDA 510(k) clearance on 1977-03-01. The listed applicant is Litton Medical Systems. The 510(k) number is K770336.

When did X-RAY TUBE, ROTATING ANODE receive FDA 510(k) clearance?

X-RAY TUBE, ROTATING ANODE received FDA 510(k) clearance on 1977-03-01, under 510(k) number K770336.

Who is the listed applicant for X-RAY TUBE, ROTATING ANODE?

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

What is the FDA product code for X-RAY TUBE, ROTATING ANODE?

The FDA product code for X-RAY TUBE, ROTATING ANODE is ITY.

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Other records listing Litton Medical Systems 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.

K770338X-RAY CONTROL & X-RAY HV GENERATORK770334TILTING X-RAY TABLEK770337FLUOROSCOPIC ASSEMBLY, IMAGE INTENS.K770333FLUOROSCOPE, C-ARMK770335COLLIMATOR, AUTOMATICK760569THREE PHASE X-RAY CONTROLS & HV GENERATORS

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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.

K000052X-RAY MONOBLOCK, MONOBLOCK XRS-60-330Dynarad Corp.K933162MRX-750Mrx Corp.K923094MOLYBDENUMSoutheastern Medical Diagnostics, Inc.K923141PHILIPS PRE-FILTER OPTIONPhilips Medical Systems, Inc.K921129MRX-700Mrx-Ray Tube Corp.K921130MRX-865Mrx-Ray Tube 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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