Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

VIDAR DENTAL FILM DIGITIZER

K-Number: K093809 · 2010-01-07

ApplicantVidar Systems Corp.
Decision Date2010-01-07
Product CodeLMA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIDAR DENTAL FILM DIGITIZER is the device name listed in this FDA 510(k) record. The listed applicant is Vidar Systems Corp.. It received FDA 510(k) clearance on 2010-01-07 under 510(k) number K093809. 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 VIDAR DENTAL FILM DIGITIZER?

VIDAR DENTAL FILM DIGITIZER is a medical device that received FDA 510(k) clearance on 2010-01-07. The listed applicant is Vidar Systems Corp.. The 510(k) number is K093809.

When did VIDAR DENTAL FILM DIGITIZER receive FDA 510(k) clearance?

VIDAR DENTAL FILM DIGITIZER received FDA 510(k) clearance on 2010-01-07, under 510(k) number K093809.

Who is the listed applicant for VIDAR DENTAL FILM DIGITIZER?

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

What is the FDA product code for VIDAR DENTAL FILM DIGITIZER?

The FDA product code for VIDAR DENTAL FILM DIGITIZER is LMA.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Vidar Systems 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.

K130636TELERADPRO EDGE; TELERADPRO EDGE HD-CCDK130406DIAGNOSTICPRO EDGEK102476TELERADPROK071193VIDAR VISION 3000 AND 4000 X-RAY SYSTEMSK070563VIDAR VISION 2000K024171VIDAR BONE TRACK SYSTEM SOFTWARE

View all 13 devices →

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.K091288MEDI-6000 MEDICAL IMAGE DIGITIZERMicrotek International, Inc.K063424FILM DIGITZER, MODEL 2908 MAMMO PROArray Corp.

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.

↑