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FDA 510(k)

MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATOR

K-Number: K952265 · 1995-07-06

ApplicantControl-X, Inc.
Decision Date1995-07-06
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Control-X, Inc.. It received FDA 510(k) clearance on 1995-07-06 under 510(k) number K952265. The device is classified under product code IZO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATOR?

MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATOR is a medical device that received FDA 510(k) clearance on 1995-07-06. The listed applicant is Control-X, Inc.. The 510(k) number is K952265.

When did MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATOR receive FDA 510(k) clearance?

MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATOR received FDA 510(k) clearance on 1995-07-06, under 510(k) number K952265.

Who is the listed applicant for MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATOR?

The FDA 510(k) record lists Control-X, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATOR?

The FDA product code for MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATOR is IZO.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Control-X, 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.

K920347TOP-X 650HF RADIOGRAPHIC X-RAYK924445BA-4 WALL BUCKY AND BA-42 TILTING WALL BUCKYK920349PCX 1050HF RADIOGRAPHIC X-RAY GENERATORK920351PCX 650HF RADIOGRAPHIC X-RAYK924444B-4 FOUR-WAY RADIOGRAPHIC TABLEK924443RS-3 UNIVERSAL RADIOGRAPHIC WORKING PLACE

View all 9 devices →

Related Devices (Code: IZO)

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.

K954666MPH50, MPH65, AND MPH80GE Medical SystemsK953582HFX350, 30KW, 300MA, 1 OR 3 PHASE RADIOGRAPHIC & FLUOROSCOPIC X-RAY GENERATORVarian Canada, Inc.K953831N 800 HFNucletron-Oldelft Corp.K952822SHIMADZU X-RAY HIGH VILTAGE GENERATOR AHD150GShimadzu Corp.K950883POLYDOROS SX 65 AND 80Siemens Medical Solutions USA, Inc.K950694COMPACT-XElectromed Intl., 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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