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FDA 510(k)

SPECTRUM MARK I SPECIAL PROCEDURES TABLE

K-Number: K931563 · 1993-08-23

ApplicantSpectrum X-Ray Corp.
Decision Date1993-08-23
Product CodeIXR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SPECTRUM MARK I SPECIAL PROCEDURES TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Spectrum X-Ray Corp.. It received FDA 510(k) clearance on 1993-08-23 under 510(k) number K931563. 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 SPECTRUM MARK I SPECIAL PROCEDURES TABLE?

SPECTRUM MARK I SPECIAL PROCEDURES TABLE is a medical device that received FDA 510(k) clearance on 1993-08-23. The listed applicant is Spectrum X-Ray Corp.. The 510(k) number is K931563.

When did SPECTRUM MARK I SPECIAL PROCEDURES TABLE receive FDA 510(k) clearance?

SPECTRUM MARK I SPECIAL PROCEDURES TABLE received FDA 510(k) clearance on 1993-08-23, under 510(k) number K931563.

Who is the listed applicant for SPECTRUM MARK I SPECIAL PROCEDURES TABLE?

The FDA 510(k) record lists Spectrum X-Ray Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPECTRUM MARK I SPECIAL PROCEDURES TABLE?

The FDA product code for SPECTRUM MARK I SPECIAL PROCEDURES TABLE is IXR.

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Other records listing Spectrum X-Ray Corp. 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.

K933134SPECTRUM DG-P7000 PEDIATRIC CRADLEK870707PENTAMAX 1 MODEL B TABLE SYSTEMK834494SPECTRUM X-RAY CORPK840463DIGITAL CRADLEK827450SIMPLAMATIC IIIK813561SPECTRUM PEDIATRIC CARDLE TABLE

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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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