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FDA 510(k)

PHILIPS XRG 90 X-RAY GENERATOR SYSTEM

K-Number: K933650 · 1993-10-07

ApplicantPhilips Medical Systems North America, Inc.
Decision Date1993-10-07
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHILIPS XRG 90 X-RAY GENERATOR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems North America, Inc.. It received FDA 510(k) clearance on 1993-10-07 under 510(k) number K933650. 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 PHILIPS XRG 90 X-RAY GENERATOR SYSTEM?

PHILIPS XRG 90 X-RAY GENERATOR SYSTEM is a medical device that received FDA 510(k) clearance on 1993-10-07. The listed applicant is Philips Medical Systems North America, Inc.. The 510(k) number is K933650.

When did PHILIPS XRG 90 X-RAY GENERATOR SYSTEM receive FDA 510(k) clearance?

PHILIPS XRG 90 X-RAY GENERATOR SYSTEM received FDA 510(k) clearance on 1993-10-07, under 510(k) number K933650.

Who is the listed applicant for PHILIPS XRG 90 X-RAY GENERATOR SYSTEM?

The FDA 510(k) record lists Philips Medical Systems North America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHILIPS XRG 90 X-RAY GENERATOR SYSTEM?

The FDA product code for PHILIPS XRG 90 X-RAY GENERATOR SYSTEM is IZO.

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Other records listing Philips Medical Systems North America, 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.

K102005ALLURA XPER OR TABLE SERIESK062233HEARTSTART MRX MONITOR/DEFIBRILLATORK062283THE PHILIPS MP20, MP30, MP40, MP50, MP60, MP70, MP80, MP90 INTELLIVUE PATIENT MONITORSK061052THE PHILIPS INTELLIVUE PATIENT MONITORS, MODELS MP20,MP30,MP40,MP50,MP60,MP70,MP80,MP90K050151MULTIDIAGNOST ELEVAK042867PHILIPS ORTHOPAEDIC APPLICATIONS

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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.K952265MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATORControl-X, Inc.K950883POLYDOROS SX 65 AND 80Siemens Medical Solutions USA, 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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