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FDA 510(k)

KODAK EKTASCAN LASER PRINTER, MODEL 100

K-Number: K863629 · 1986-10-27

ApplicantEastman Kodak Company
Decision Date1986-10-27
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK EKTASCAN LASER PRINTER, MODEL 100 is the device name listed in this FDA 510(k) record. The listed applicant is Eastman Kodak Company. It received FDA 510(k) clearance on 1986-10-27 under 510(k) number K863629. The device is classified under product code LMC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK EKTASCAN LASER PRINTER, MODEL 100?

KODAK EKTASCAN LASER PRINTER, MODEL 100 is a medical device that received FDA 510(k) clearance on 1986-10-27. The listed applicant is Eastman Kodak Company. The 510(k) number is K863629.

When did KODAK EKTASCAN LASER PRINTER, MODEL 100 receive FDA 510(k) clearance?

KODAK EKTASCAN LASER PRINTER, MODEL 100 received FDA 510(k) clearance on 1986-10-27, under 510(k) number K863629.

Who is the listed applicant for KODAK EKTASCAN LASER PRINTER, MODEL 100?

The FDA 510(k) record lists Eastman Kodak Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KODAK EKTASCAN LASER PRINTER, MODEL 100?

The FDA product code for KODAK EKTASCAN LASER PRINTER, MODEL 100 is LMC.

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Related Devices (Code: LMC)

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.

K111566DRYVIEW CHROMA IMAGING SYSTEMCarestream Health, Inc.K092280CYPHER DICOM PRINT SOLUTIONVirtual Imaging, Inc.K090469CARESTREAM DRYVIEW 5850 LASER IMAGERCarestream Health, Inc.K083522SONY UP-DF750 DIGITAL FILM IMAGERSony Electronics, Inc.K081637LASER IMAGER DRYPRO MODEL 873Konica Minolta Medical & Graphic, Inc.K072680DRYSTAR AXYS, MODEL EYZ4EAgfa Healthcare Corporation

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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