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)

MATRIS INSTRU. VIDEO IMAGER 1010-

K-Number: K842494 · 1984-08-17

ApplicantMatrix Instruments
Decision Date1984-08-17
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MATRIS INSTRU. VIDEO IMAGER 1010- is the device name listed in this FDA 510(k) record. The listed applicant is Matrix Instruments. It received FDA 510(k) clearance on 1984-08-17 under 510(k) number K842494. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATRIS INSTRU. VIDEO IMAGER 1010-?

MATRIS INSTRU. VIDEO IMAGER 1010- is a medical device that received FDA 510(k) clearance on 1984-08-17. The listed applicant is Matrix Instruments. The 510(k) number is K842494.

When did MATRIS INSTRU. VIDEO IMAGER 1010- receive FDA 510(k) clearance?

MATRIS INSTRU. VIDEO IMAGER 1010- received FDA 510(k) clearance on 1984-08-17, under 510(k) number K842494.

Who is the listed applicant for MATRIS INSTRU. VIDEO IMAGER 1010-?

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 MATRIS INSTRU. VIDEO IMAGER 1010-?

The FDA product code for MATRIS INSTRU. VIDEO IMAGER 1010- is IZI.

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.

K860777MATRIX LD & LD/LASER DIGITIZERK860776MATRIX LR, LR 22A & LR/LASER RECORDERK842495MATRIX VIDEO IMAGER 1020 COMPACT CAMER

Related Devices (Code: IZI)

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.

K261037780 nm SPY Portable Handheld Imaging (SPY-PHI) SystemStryker EndoscopyK253181SURGIMAGE SIM 1000H Fluorescence Imaging PlatformSurgimage CorporationK243645IC-Flow™ Imaging System 2.0Diagnostic Green GmbHK243077Affirm 800Digital Surgery Systems, Inc. (D.B.A True Digital Surgery)K231986Modus IRSynaptive Medical, Inc.K234090EXPLORER AIR® II (8001, 8002, 8003); EXPLORER AIR® Sterile Drape (8004)Surgvision GmbH

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.

↑