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FDA 510(k)

URO - ELITE TABLE ACCESSORIES

K-Number: K944987 · 1994-11-30

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1994-11-30
Product CodeIXR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

URO - ELITE TABLE ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 1994-11-30 under 510(k) number K944987. The device is classified under product code IXR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URO - ELITE TABLE ACCESSORIES?

URO - ELITE TABLE ACCESSORIES is a medical device that received FDA 510(k) clearance on 1994-11-30. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K944987.

When did URO - ELITE TABLE ACCESSORIES receive FDA 510(k) clearance?

URO - ELITE TABLE ACCESSORIES received FDA 510(k) clearance on 1994-11-30, under 510(k) number K944987.

Who is the listed applicant for URO - ELITE TABLE ACCESSORIES?

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

What is the FDA product code for URO - ELITE TABLE ACCESSORIES?

The FDA product code for URO - ELITE TABLE ACCESSORIES is IXR.

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Related Devices (Code: IXR)

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.

K000412VISION R/F TILTING TABLEVilla Sistemi Medicali S.P.A.K973039LEGACY/LEGACY-D TABLEGE Medical SystemsK971128CAP-35B III/CINE 275Jamieson Film Co.K970640PHILIPS EASY DIAGNOSTPhilips Medical Systems North America, Inc.K965105ELECTROPHYSIOLOGY TILT TABLE MODEL #9660U.S. Imaging Tables, Inc.K965096FLUOROVIEW SERIES FLUOROSCOPIC TABLESU.S. Imaging Tables, 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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