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FDA 510(k)

CEMAX SCANLINK V

K-Number: K943357 · 1994-11-22

ApplicantCemax, Inc.
Decision Date1994-11-22
Product CodeLMA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CEMAX SCANLINK V is the device name listed in this FDA 510(k) record. The listed applicant is Cemax, Inc.. It received FDA 510(k) clearance on 1994-11-22 under 510(k) number K943357. 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 CEMAX SCANLINK V?

CEMAX SCANLINK V is a medical device that received FDA 510(k) clearance on 1994-11-22. The listed applicant is Cemax, Inc.. The 510(k) number is K943357.

When did CEMAX SCANLINK V receive FDA 510(k) clearance?

CEMAX SCANLINK V received FDA 510(k) clearance on 1994-11-22, under 510(k) number K943357.

Who is the listed applicant for CEMAX SCANLINK V?

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

What is the FDA product code for CEMAX SCANLINK V?

The FDA product code for CEMAX SCANLINK V is LMA.

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Other records listing Cemax, 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.

K950513ARCHIVEMANAGERK945188CEMAX VIPSTATION AND/OR SOFTWAREK932371CEMAX CLINICALVIEW(TM) STATION AND/OR SOFTWAREK932372CEMAX VIPSTATION(TM) AND/OR SOFTWAREK905801CEMAX SPARCSTATION IMAGING SOFTWARE AND WORKSTATIOK880169CEMAX 5000 MULTIDIMENSIONAL IMAGING WORKSTATION

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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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