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FDA 510(k)

KONICA LD-4500 LASER DIGITIZER

K-Number: K933830 · 1993-12-14

ApplicantKonica Medical Corp.
Decision Date1993-12-14
Product CodeLMA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KONICA LD-4500 LASER DIGITIZER is the device name listed in this FDA 510(k) record. The listed applicant is Konica Medical Corp.. It received FDA 510(k) clearance on 1993-12-14 under 510(k) number K933830. The device is classified under product code LMA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KONICA LD-4500 LASER DIGITIZER?

KONICA LD-4500 LASER DIGITIZER is a medical device that received FDA 510(k) clearance on 1993-12-14. The listed applicant is Konica Medical Corp.. The 510(k) number is K933830.

When did KONICA LD-4500 LASER DIGITIZER receive FDA 510(k) clearance?

KONICA LD-4500 LASER DIGITIZER received FDA 510(k) clearance on 1993-12-14, under 510(k) number K933830.

Who is the listed applicant for KONICA LD-4500 LASER DIGITIZER?

The FDA 510(k) record lists Konica Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KONICA LD-4500 LASER DIGITIZER?

The FDA product code for KONICA LD-4500 LASER DIGITIZER is LMA.

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Other records listing Konica Medical 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.

K990969KONICA SRX- 701 AUTOMATIC X-RAY FILM PROCESSORK963914CM & CM DS-7K963913MD100 & MM150K955583VIFSK931315KONICA SRX-501A AUTOMATIC X-RAY FILM PROCESSORK931316KONICA DS-7 AUTOMATIC X-RAY FILM PROCESSOR

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Related Devices (Code: LMA)

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.

K132183DICOM VIDEOBar Code Computer, Ltd.K130636TELERADPRO EDGE; TELERADPRO EDGE HD-CCDVidar Systems Corp.K130406DIAGNOSTICPRO EDGEVidar Systems Corp.K102476TELERADPROVidar Systems Corp.K093809VIDAR DENTAL FILM DIGITIZERVidar Systems Corp.K091288MEDI-6000 MEDICAL IMAGE DIGITIZERMicrotek International, 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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