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FDA 510(k)

RS-3 UNIVERSAL RADIOGRAPHIC WORKING PLACE

K-Number: K924443 · 1993-02-05

ApplicantControl-X, Inc.
Decision Date1993-02-05
Product CodeIZF
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RS-3 UNIVERSAL RADIOGRAPHIC WORKING PLACE 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 1993-02-05 under 510(k) number K924443. The device is classified under product code IZF. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RS-3 UNIVERSAL RADIOGRAPHIC WORKING PLACE?

RS-3 UNIVERSAL RADIOGRAPHIC WORKING PLACE is a medical device that received FDA 510(k) clearance on 1993-02-05. The listed applicant is Control-X, Inc.. The 510(k) number is K924443.

When did RS-3 UNIVERSAL RADIOGRAPHIC WORKING PLACE receive FDA 510(k) clearance?

RS-3 UNIVERSAL RADIOGRAPHIC WORKING PLACE received FDA 510(k) clearance on 1993-02-05, under 510(k) number K924443.

Who is the listed applicant for RS-3 UNIVERSAL RADIOGRAPHIC WORKING PLACE?

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 RS-3 UNIVERSAL RADIOGRAPHIC WORKING PLACE?

The FDA product code for RS-3 UNIVERSAL RADIOGRAPHIC WORKING PLACE is IZF.

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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.

K952265MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATORK920347TOP-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 TABLE

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Related Devices (Code: IZF)

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.

K252649TAP2DNano-X Imaging , Ltd.K252133Adaptix Ortho350Adaptix LimitedK250850Nanox.ARC XNano-X Imaging , Ltd.K242395Nanox.ARCNano-X Imaging , Ltd.K222934Nanox.ARCNano-X Imaging , Ltd.K221949Ortho Device, ADAPTIX 3D Orthopedic Imaging SystemPausch Medical GmbH

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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