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FDA 510(k)

14X14 MULTIFORMAT SPOT FILMER, NO. 6650.400

K-Number: K881589 · 1988-07-18

ApplicantContinental X-Ray Corp.
Decision Date1988-07-18
Product CodeIXL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

14X14 MULTIFORMAT SPOT FILMER, NO. 6650.400 is the device name listed in this FDA 510(k) record. The listed applicant is Continental X-Ray Corp.. It received FDA 510(k) clearance on 1988-07-18 under 510(k) number K881589. The device is classified under product code IXL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 14X14 MULTIFORMAT SPOT FILMER, NO. 6650.400?

14X14 MULTIFORMAT SPOT FILMER, NO. 6650.400 is a medical device that received FDA 510(k) clearance on 1988-07-18. The listed applicant is Continental X-Ray Corp.. The 510(k) number is K881589.

When did 14X14 MULTIFORMAT SPOT FILMER, NO. 6650.400 receive FDA 510(k) clearance?

14X14 MULTIFORMAT SPOT FILMER, NO. 6650.400 received FDA 510(k) clearance on 1988-07-18, under 510(k) number K881589.

Who is the listed applicant for 14X14 MULTIFORMAT SPOT FILMER, NO. 6650.400?

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

What is the FDA product code for 14X14 MULTIFORMAT SPOT FILMER, NO. 6650.400?

The FDA product code for 14X14 MULTIFORMAT SPOT FILMER, NO. 6650.400 is IXL.

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Other records listing Continental 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.

K972442CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002K962140ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM MODEL NO. 6896.300K961690CARDIOARC SERIES: POSITIONER C-ARM MODELS NO. 6896.001 AND 6896.105K954581ARC SERIESK950571LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270K942175LINEAR TOMOGRAPHIC SYSTEM: PMT 6000

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Related Devices (Code: IXL)

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.

K111304OPTIMA XR120Ge Medical Systems, LLCK964806MD-1835Fischer Imaging Corp.K950317ADVANTX 1824 SPOTFILM DEVICEGE Medical SystemsK940386KODAK AUTOMIXER III INTEGRATED, KODAK AUTOMIXER III 180 LPEastman Kodak CompanyK942367AXT 1400 SPOTFILM DEVICEApplied X-Ray Technologies, Inc.K924593DIAGNOST 76 FAMILY*R/F SYSTEMS - RELEASE 4.4Philips Medical Systems, 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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