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FDA 510(k)

MATRIX LD & LD/LASER DIGITIZER

K-Number: K860777 · 1987-04-22

ApplicantMatrix Instruments
Decision Date1987-04-22
Product CodeLMA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MATRIX LD & LD/LASER DIGITIZER is the device name listed in this FDA 510(k) record. The listed applicant is Matrix Instruments. It received FDA 510(k) clearance on 1987-04-22 under 510(k) number K860777. 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 MATRIX LD & LD/LASER DIGITIZER?

MATRIX LD & LD/LASER DIGITIZER is a medical device that received FDA 510(k) clearance on 1987-04-22. The listed applicant is Matrix Instruments. The 510(k) number is K860777.

When did MATRIX LD & LD/LASER DIGITIZER receive FDA 510(k) clearance?

MATRIX LD & LD/LASER DIGITIZER received FDA 510(k) clearance on 1987-04-22, under 510(k) number K860777.

Who is the listed applicant for MATRIX LD & LD/LASER DIGITIZER?

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

What is the FDA product code for MATRIX LD & LD/LASER DIGITIZER?

The FDA product code for MATRIX LD & LD/LASER 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 Matrix Instruments 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.

K860776MATRIX LR, LR 22A & LR/LASER RECORDERK842495MATRIX VIDEO IMAGER 1020 COMPACT CAMERK842494MATRIS INSTRU. VIDEO IMAGER 1010-

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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