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FDA 510(k)

COMPACT LASER IMAGER, MODEL CLI-100

K-Number: K902347 · 1991-03-04

ApplicantLumisys, Inc.
Decision Date1991-03-04
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COMPACT LASER IMAGER, MODEL CLI-100 is the device name listed in this FDA 510(k) record. The listed applicant is Lumisys, Inc.. It received FDA 510(k) clearance on 1991-03-04 under 510(k) number K902347. 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 COMPACT LASER IMAGER, MODEL CLI-100?

COMPACT LASER IMAGER, MODEL CLI-100 is a medical device that received FDA 510(k) clearance on 1991-03-04. The listed applicant is Lumisys, Inc.. The 510(k) number is K902347.

When did COMPACT LASER IMAGER, MODEL CLI-100 receive FDA 510(k) clearance?

COMPACT LASER IMAGER, MODEL CLI-100 received FDA 510(k) clearance on 1991-03-04, under 510(k) number K902347.

Who is the listed applicant for COMPACT LASER IMAGER, MODEL CLI-100?

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

What is the FDA product code for COMPACT LASER IMAGER, MODEL CLI-100?

The FDA product code for COMPACT LASER IMAGER, MODEL CLI-100 is LMC.

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Other records listing Lumisys, 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.

K980809LUMISCAN 135 PHOSPHOR PLATE DIGITIZER/LUMISYS 135 ERASERK980213DI-2000K953371LUMISYS DICOM TOOKLITK953964LUMISYS, LUMISCAN 20K933129LUMISCAN 50K901423DIGITAL IMAGE SCANNER, MODEL DIS-1000

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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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