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FDA 510(k)

KONICA KFDR-S

K-Number: K896739 · 1990-04-30

ApplicantKonica Medical Corp.
Decision Date1990-04-30
Product CodeLMA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KONICA KFDR-S 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 1990-04-30 under 510(k) number K896739. 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 KFDR-S?

KONICA KFDR-S is a medical device that received FDA 510(k) clearance on 1990-04-30. The listed applicant is Konica Medical Corp.. The 510(k) number is K896739.

When did KONICA KFDR-S receive FDA 510(k) clearance?

KONICA KFDR-S received FDA 510(k) clearance on 1990-04-30, under 510(k) number K896739.

Who is the listed applicant for KONICA KFDR-S?

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 KFDR-S?

The FDA product code for KONICA KFDR-S 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 PROCESSORK963913MD100 & MM150K963914CM & CM DS-7K955583VIFSK931316KONICA DS-7 AUTOMATIC X-RAY FILM PROCESSORK931317KONICA SRX-301 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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